{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T11:49:01Z","timestamp":1790768941064,"version":"4.1.0"},"reference-count":107,"publisher":"Elsevier","isbn-type":[{"value":"9780128171318","type":"print"}],"license":[{"start":{"date-parts":[[2022,1,1]],"date-time":"2022-01-01T00:00:00Z","timestamp":1640995200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2022,1,1]],"date-time":"2022-01-01T00:00:00Z","timestamp":1640995200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2022,1,1]],"date-time":"2022-01-01T00:00:00Z","timestamp":1640995200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2022,1,1]],"date-time":"2022-01-01T00:00:00Z","timestamp":1640995200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2022,1,1]],"date-time":"2022-01-01T00:00:00Z","timestamp":1640995200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2022,1,1]],"date-time":"2022-01-01T00:00:00Z","timestamp":1640995200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022]]},"DOI":"10.1016\/bs.ctdb.2021.12.004","type":"book-chapter","created":{"date-parts":[[2022,3,28]],"date-time":"2022-03-28T11:25:30Z","timestamp":1648466730000},"page":"51-77","source":"Crossref","is-referenced-by-count":20,"title":["Mammalian uterine morphogenesis and variations"],"prefix":"10.1016","author":[{"given":"Diana A.","family":"Machado","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alejandra E.","family":"Ontiveros","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Richard R.","family":"Behringer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/bs.ctdb.2021.12.004_bb0010","doi-asserted-by":"crossref","first-page":"2274","DOI":"10.1002\/ajmg.a.35437","article-title":"Molecular basis of the clinical features of Al-Awadi-Raas-Rothschild (limb\/pelvis\/uterus-hypoplasia\/aplasia) syndrome (AARRS) and Fuhrmann syndrome","volume":"161A","author":"Al-Qattan","year":"2013","journal-title":"American Journal of Medical Genetics. Part A"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0015","doi-asserted-by":"crossref","first-page":"3553","DOI":"10.1093\/nar\/19.13.3553","article-title":"Two members of an HNF1 homeoprotein family are expressed in human liver","volume":"19","author":"Bach","year":"1991","journal-title":"Nucleic Acids Research"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0020","doi-asserted-by":"crossref","first-page":"4795","DOI":"10.1242\/dev.126.21.4795","article-title":"Variant hepatocyte nuclear factor 1 is required for visceral endoderm specification","volume":"126","author":"Barbacci","year":"1999","journal-title":"Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0025","doi-asserted-by":"crossref","first-page":"104158","DOI":"10.1016\/j.ejmg.2021.104158","article-title":"GREB1L as a candidate gene of Mayer-Rokitansky-Kuster-Hauser syndrome","volume":"64","author":"Barffour","year":"2021","journal-title":"European Journal of Medical Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0030","doi-asserted-by":"crossref","first-page":"168","DOI":"10.1006\/dbio.1994.1018","article-title":"Embryonic expression of Lim-1, the mouse homolog of Xenopus Xlim-1, suggests a role in lateral mesoderm differentiation and neurogenesis","volume":"161","author":"Barnes","year":"1994","journal-title":"Developmental Biology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0035","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1016\/j.theriogenology.2020.09.004","article-title":"Morphophysiological variations of the female reproductive organs of the vespertilionid bat Myotis nigricans during its different reproductive phases","volume":"158","author":"Beguelini","year":"2020","journal-title":"Theriogenology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb448","doi-asserted-by":"crossref","first-page":"510","DOI":"10.7326\/0003-4819-140-7-200404060-00009","article-title":"Clinical spectrum associated with hepatocyte nuclear factor-1B mutations","volume":"140","author":"Bellanne-Chantelot","year":"2004","journal-title":"Annals of Internal Medicine"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0040","doi-asserted-by":"crossref","DOI":"10.1016\/j.cell.2017.03.008","article-title":"Tridimensional visualization and analysis of early human development","volume":"169","author":"Belle","year":"2017","journal-title":"Cell"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb451","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1186\/1750-1172-4-25","article-title":"Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: Two case reports","volume":"4","author":"Bernardini","year":"2009","journal-title":"Orphanet Journal of Rare Diseases"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0045","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1534\/genetics.117.1125","article-title":"A gene implicated in activation of retinoic acid receptor targets is a novel renal agenesis gene in humans","volume":"207","author":"Brophy","year":"2017","journal-title":"Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0050","doi-asserted-by":"crossref","first-page":"623","DOI":"10.1007\/s003359900187","article-title":"Dlgh1, a mouse homolog of the drosophila discs-large gene, is located on chromosome 16","volume":"7","author":"Burgess","year":"1996","journal-title":"Mammalian Genome"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0055","first-page":"355","article-title":"Bicornuate uterus","volume":"67","author":"Campbell","year":"1952","journal-title":"Canadian Medical Association Journal"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0060","doi-asserted-by":"crossref","first-page":"283","DOI":"10.1016\/j.devcel.2005.05.016","article-title":"Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system","volume":"9","author":"Carroll","year":"2005","journal-title":"Developmental Cell"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0065","doi-asserted-by":"crossref","first-page":"1475","DOI":"10.1128\/MCB.21.5.1475-1483.2001","article-title":"Craniofacial dysmorphogenesis including cleft palate in mice with an insertional mutation in the discs large gene","volume":"21","author":"Caruana","year":"2001","journal-title":"Molecular and Cellular Biology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0070","doi-asserted-by":"crossref","first-page":"761","DOI":"10.1093\/humupd\/dmr028","article-title":"The prevalence of congenital uterine anomalies in unselected and high-risk populations: A systematic review","volume":"17","author":"Chan","year":"2011","journal-title":"Human Reproduction Update"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0075","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1016\/j.ajhg.2020.12.014","article-title":"Perturbations of genes essential for Mullerian duct and Wolffian duct development in Mayer-Rokitansky-Kuster-Hauser syndrome","volume":"108","author":"Chen","year":"2021","journal-title":"American Journal of Human Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb450","doi-asserted-by":"crossref","unstructured":"Cheroki C., Krepischi-Santos A.C.V., Szuhai K., Brenner V., Kim C.A.E., Otto P.A., et al., 2008. Genomic imbalances associated with mullerian aplasia, Journal of Medical Genetics, 45 (4), 228-232, 10.1136\/jmg.2007.051839. Epub 2007 Nov 26","DOI":"10.1136\/jmg.2007.051839"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0080","doi-asserted-by":"crossref","first-page":"721","DOI":"10.1002\/dvdy.20400","article-title":"Embryonic staging system for the short-tailed fruit bat, Carollia perspicillata, a model organism for the mammalian order Chiroptera, based upon timed pregnancies in captive-bred animals","volume":"233","author":"Cretekos","year":"2005","journal-title":"Developmental Dynamics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0090","doi-asserted-by":"crossref","first-page":"46","DOI":"10.1016\/j.diff.2018.09.001","article-title":"Development of the human female reproductive tract","volume":"103","author":"Cunha","year":"2018","journal-title":"Differentiation"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0085","doi-asserted-by":"crossref","first-page":"417","DOI":"10.1679\/aohc.67.417","article-title":"Role of stromal-epithelial interactions in hormonal responses","volume":"67","author":"Cunha","year":"2004","journal-title":"Archives of Histology and Cytology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0095","doi-asserted-by":"crossref","first-page":"166","DOI":"10.5694\/j.1326-5377.1949.tb36722.x","article-title":"Bicornuate uterus","volume":"2","author":"Davies","year":"1949","journal-title":"The Medical Journal of Australia"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb453","doi-asserted-by":"crossref","unstructured":"De Arcangelis A, Mark M, Kreidberg J, Sorokin L, Georges-Labouesse E., 1999. Synergistic activities of alpha3 and alpha6 integrins are required during apical ectodermal ridge formation and organogenesis in the mouse. Development 126 (17), 3957-3968. doi: 10.1242\/dev.126.17.3957. PMID: 10433923","DOI":"10.1242\/dev.126.17.3957"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0100","doi-asserted-by":"crossref","first-page":"803","DOI":"10.1016\/j.ajhg.2017.09.026","article-title":"Mutations in GREB1L cause bilateral kidney agenesis in humans and mice","volume":"101","author":"De Tomasi","year":"2017","journal-title":"American Journal of Human Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0105","doi-asserted-by":"crossref","first-page":"227","DOI":"10.1016\/j.ydbio.2007.04.036","article-title":"Essential roles of mesenchyme-derived beta-catenin in mouse Mullerian duct morphogenesis","volume":"307","author":"Deutscher","year":"2007","journal-title":"Developmental Biology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0110","doi-asserted-by":"crossref","first-page":"787","DOI":"10.1242\/dev.109.4.787","article-title":"Pax2, a new murine paired-box-containing gene and its expression in the developing excretory system","volume":"109","author":"Dressler","year":"1990","journal-title":"Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb457","doi-asserted-by":"crossref","unstructured":"Eyaid W., Al-Qattan M.M., Al Abdulkareem I., Fetaini N., Al Balwi M., 2011. A novel homozygous missense mutation (c.610G>A, p.Gly204Ser) in the WNT7A gene causes tetra-amelia in two Saudi families. The American Journal of Medical Genetics, 155A (3):599-604. doi: 10.1002\/ajmg.a.33717. Epub 2011 Feb 22.PMID: 21344627","DOI":"10.1002\/ajmg.a.33717"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0115","doi-asserted-by":"crossref","first-page":"R86","DOI":"10.1186\/gb-2011-12-9-r86","article-title":"Mutation discovery in mice by whole exome sequencing","volume":"12","author":"Fairfield","year":"2011","journal-title":"Genome Biology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0120","doi-asserted-by":"crossref","first-page":"233","DOI":"10.1111\/cge.12883","article-title":"Genetics of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome","volume":"91","author":"Fontana","year":"2017","journal-title":"Clinical Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0125","doi-asserted-by":"crossref","first-page":"73","DOI":"10.1002\/aja.1001990108","article-title":"Expression patterns of the murine LIM class homeobox gene lim1 in the developing brain and excretory system","volume":"199","author":"Fujii","year":"1994","journal-title":"Developmental Dynamics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb458","doi-asserted-by":"crossref","unstructured":"Garavelli L, Wischmeijer A, Rosato S, Gelmini C, Reverberi S, Sassi S, et al., 2011. Al-Awadi-Raas-Rothschild (limb\/pelvis\/uterus-hypoplasia\/aplasia) syndrome and WNT7A mutations: genetic homogeneity and nosological delineation. The American Journal of Medical Genetics. 155A (2):332-336. doi: 10.1002\/ajmg.a.33793. Epub 2010 Dec 22.PMID: 21271649","DOI":"10.1002\/ajmg.a.33793"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb454","unstructured":"Ghyselinck NB, Dup\u00e9 V, Dierich A, Messaddeq N, Garnier JM, Rochette-Egly C, et al., 1997. Role of the retinoic acid receptor beta (RARbeta) during mouse development. The International Journal of Developmental Biology 41 (3), 425-447. PMID: 9240560"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb460","doi-asserted-by":"crossref","unstructured":"Goodman F.R., Bacchelli C., Brady A.F., Brueton L.A., Fryns J.P., Mortlock D.P., et al., 2000. Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome. The American Journal of Human Genetics 67 (1), 197-202. doi: 10.1086\/302961. Epub 2000 Jun 5.PMID: 10839976","DOI":"10.1086\/302961"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0130","doi-asserted-by":"crossref","first-page":"786","DOI":"10.1007\/BF00582219","article-title":"Zur Entwicklungsmechanik des Urogenitalsystems beim Huhn","volume":"136","author":"Gr\u00fcnwald","year":"1937","journal-title":"Wilhelm Roux' Archiv f\u00fcr Entwicklungsmechanik der Organismen"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0135","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1016\/j.ydbio.2006.09.046","article-title":"The origin of the Mullerian duct in chick and mouse","volume":"302","author":"Guioli","year":"2007","journal-title":"Developmental Biology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0140","series-title":"Reproduction and breeding techniques for laboratory animals","author":"Hafez","year":"1970"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0145","doi-asserted-by":"crossref","first-page":"308","DOI":"10.1095\/biolreprod.110.088161","article-title":"WNTs in the neonatal mouse uterus: Potential regulation of endometrial gland development","volume":"84","author":"Hayashi","year":"2011","journal-title":"Biology of Reproduction"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0150","doi-asserted-by":"crossref","first-page":"1838","DOI":"10.1093\/humrep\/dez126","article-title":"Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Mullerian and renal agenesis: A novel candidate gene in Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome. A case report","volume":"34","author":"Herlin","year":"2019","journal-title":"Human Reproduction"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0155","doi-asserted-by":"crossref","first-page":"124","DOI":"10.1016\/j.ydbio.2014.01.025","article-title":"Lhx1 is required in Mullerian duct epithelium for uterine development","volume":"389","author":"Huang","year":"2014","journal-title":"Developmental Biology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0160","doi-asserted-by":"crossref","first-page":"1799","DOI":"10.1242\/dev.02830","article-title":"Abnormal development of urogenital organs in Dlgh1-deficient mice","volume":"134","author":"Iizuka-Kogo","year":"2007","journal-title":"Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0165","series-title":"Hand-foot-genital syndrome","author":"Innis","year":"1993"},{"key":"#cr-split#-10.1016\/bs.ctdb.2021.12.004_bb461.1","unstructured":"Innis J.W., (2006). Hand-Foot-Genital Syndrome. In: Adam M.P., Ardinger H.H., Pagon R.A., Wallace S.E., Bean L.J.H., Gripp K.W., Mirzaa G.M., Amemiya A., (Eds.), GeneReviews\u00ae [Internet]. Seattle (WA): University of Washington, Seattle"},{"key":"#cr-split#-10.1016\/bs.ctdb.2021.12.004_bb461.2","unstructured":"1993-2022. PMID: 20301596. [updated 2019 Aug 8]"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0170","doi-asserted-by":"crossref","first-page":"209","DOI":"10.1016\/j.theriogenology.2018.09.035","article-title":"Severe incomplete fusion of the Mullerian ducts influences reproduction in Holstein cattle","volume":"123","author":"Ishiyama","year":"2019","journal-title":"Theriogenology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0175","doi-asserted-by":"crossref","first-page":"126","DOI":"10.1111\/cge.13769","article-title":"GREB1L variants in familial and sporadic hereditary urogenital adysplasia and Mayer-Rokitansky-Kuster-Hauser syndrome","volume":"98","author":"Jacquinet","year":"2020","journal-title":"Clinical Genetics"},{"issue":"11","key":"10.1016\/bs.ctdb.2021.12.004_bb456","doi-asserted-by":"crossref","first-page":"2832","DOI":"10.1002\/ajmg.a.33673","article-title":"A Novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi\/Raas-Rothschild\/Schinzel phocomelia syndrome","volume":"152A","author":"Kantaputra","year":"2010","journal-title":"The American Journal of Medical Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0180","first-page":"61","article-title":"Expression pattern of the rat Lim-1 homeobox gene suggests a dual role during kidney development","volume":"42","author":"Karavanov","year":"1998","journal-title":"The International Journal of Developmental Biology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0185","doi-asserted-by":"crossref","first-page":"4225","DOI":"10.1242\/dev.125.21.4225","article-title":"Wnt-4 is a mesenchymal signal for epithelial transformation of metanephric mesenchyme in the developing kidney","volume":"125","author":"Kispert","year":"1998","journal-title":"Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0190","doi-asserted-by":"crossref","first-page":"969","DOI":"10.1038\/nrg1225","article-title":"Developmental genetics of the female reproductive tract in mammals","volume":"4","author":"Kobayashi","year":"2003","journal-title":"Nature Reviews. Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0195","doi-asserted-by":"crossref","first-page":"2809","DOI":"10.1242\/dev.01858","article-title":"Distinct and sequential tissue-specific activities of the LIM-class. homeobox gene Lim1 for tubular morphogenesis during kidney development","volume":"132","author":"Kobayashi","year":"2005","journal-title":"Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0200","doi-asserted-by":"crossref","first-page":"539","DOI":"10.1242\/dev.00951","article-title":"Requirement of Lim1 for female reproductive tract development","volume":"131","author":"Kobayashi","year":"2004","journal-title":"Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0205","first-page":"61","article-title":"Development of the vagina in the human fetus","volume":"24","author":"Koff","year":"1933","journal-title":"Contributions to Embryology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0210","doi-asserted-by":"crossref","first-page":"352","DOI":"10.1002\/aja.1001780407","article-title":"Reproductive-biology of the male little mastiff bat, Mormopterus-Planiceps (Chiroptera, Molossidae), in Southeast Australia","volume":"178","author":"Krutzsch","year":"1987","journal-title":"The American Journal of Anatomy"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0215","doi-asserted-by":"crossref","first-page":"10157","DOI":"10.1074\/jbc.M309843200","article-title":"Human homolog of disc-large is required for adherens junction assembly and differentiation of human intestinal epithelial cells","volume":"279","author":"Laprise","year":"2004","journal-title":"The Journal of Biological Chemistry"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0220","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1007\/s11825-018-0173-7","article-title":"Clinical and genetic aspects of Mayer-Rokitansky-Kuster-Hauser syndrome","volume":"30","author":"Ledig","year":"2018","journal-title":"Medizinische Genetik: Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb452","doi-asserted-by":"crossref","unstructured":"Ledig S., Brucker S., Barresi G., Schomburg J., Rall K., Wieacker P., 2012. Frame shift mutation of LHX1 is associated with Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome. Human Reproduction 27 (9), 2872-2875. doi: 10.1093\/humrep\/des206. Epub 2012 Jun 26.PMID: 22740494","DOI":"10.1093\/humrep\/des206"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb463","doi-asserted-by":"crossref","unstructured":"Liang H.I., Fu S.C., Yin C.H., Chang C.C., 2020. Herlyn-Werner-Wunderlich syndrome: An unusual case with presentation of menorrhagia. Taiwanese Journal of Obstetrics and Gynecology 59 (6), 948-951. doi: 10.1016\/j.tjog.2020.09.026.PMID: 33218419","DOI":"10.1016\/j.tjog.2020.09.026"},{"issue":"11","key":"10.1016\/bs.ctdb.2021.12.004_bb449","doi-asserted-by":"crossref","first-page":"2001","DOI":"10.1093\/hmg\/8.11.2001","article-title":"A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1beta","volume":"8","author":"Lindner","year":"1999","journal-title":"Human Molecular Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0225","doi-asserted-by":"crossref","first-page":"505","DOI":"10.17219\/acem\/118850","article-title":"Mayer-Rokitansky-Kuster-Hauser syndrome as an interdisciplinary problem","volume":"29","author":"Liszewska-Kaplon","year":"2020","journal-title":"Advances in Clinical and Experimental Medicine"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0230","doi-asserted-by":"crossref","first-page":"2061","DOI":"10.1242\/dev.01090","article-title":"Wnt5a is required for proper epithelial-mesenchymal interactions in the uterus","volume":"131","author":"Mericskay","year":"2004","journal-title":"Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0235","series-title":"Capybara: Biology, Use and Conservation of an Exceptional Neotropical Species","first-page":"131","article-title":"Morphology and reproductive physiology of female capybaras","author":"Miglino","year":"2013"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0240","doi-asserted-by":"crossref","first-page":"667","DOI":"10.1007\/s00439-020-02239-y","article-title":"Genetics of agenesis\/hypoplasia of the uterus and vagina: Narrowing down the number of candidate genes for Mayer-Rokitansky-Kuster-Hauser syndrome","volume":"140","author":"Mikhael","year":"2021","journal-title":"Human Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb455","doi-asserted-by":"crossref","unstructured":"Miller C, Sassoon DA., 1998. Wnt-7a maintains appropriate uterine patterning during the development of the mouse female reproductive tract. Development 125 (16), 3201-3211. doi: 10.1242\/dev.125.16.3201.PMID: 9671592","DOI":"10.1242\/dev.125.16.3201"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0245","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1016\/S0925-4773(98)00112-9","article-title":"Differential expression patterns of Wnt genes in the murine female reproductive tract during development and the estrous cycle","volume":"76","author":"Miller","year":"1998","journal-title":"Mechanisms of Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0250","doi-asserted-by":"crossref","first-page":"2577","DOI":"10.1101\/gad.10.20.2577","article-title":"Genetic analysis of the Mullerian-inhibiting substance signal transduction pathway in mammalian sexual differentiation","volume":"10","author":"Mishina","year":"1996","journal-title":"Genes & Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb462","doi-asserted-by":"crossref","unstructured":"Mittal R.J., 2016. Herlyn-Werner-Wunderlich Syndrome, The Journal of Obstetrics and Gynecology of India (JOGI) 66 (2):128-130. doi: 10.1007\/s13224-015-0707-8. Epub 2015 May 16.PMID: 27046969","DOI":"10.1007\/s13224-015-0707-8"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0255","doi-asserted-by":"crossref","first-page":"1653","DOI":"10.1242\/dev.124.9.1653","article-title":"Defects of urogenital development in mice lacking Emx2","volume":"124","author":"Miyamoto","year":"1997","journal-title":"Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0260","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1002\/ar.b.20002","article-title":"A social biography of Carnegie embryo no. 836","volume":"276","author":"Morgan","year":"2004","journal-title":"Anatomical Record. Part B, New Anatomist"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0265","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1038\/ng0297-179","article-title":"Mutation of HOXA13 in hand-foot-genital syndrome","volume":"15","author":"Mortlock","year":"1997","journal-title":"Nature Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0270","series-title":"Vertebrate fetal membranes: Comparative ontogeny and morphology, evolution, phylogenetic significance, basic functions, research opportunities","author":"Mossman","year":"1987"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0275","doi-asserted-by":"crossref","first-page":"281","DOI":"10.1159\/000364935","article-title":"Molecular genetics of Mullerian duct formation, regression and differentiation","volume":"8","author":"Mullen","year":"2014","journal-title":"Sexual Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0280","series-title":"Bildungsgeschichte der Genitalien aus anatomischen Untersuchungen an Embryonen des Menschen und der Thiere; nebst einem Anhang \u00fcber die chirurgische Behandlung der Hypospadia","author":"M\u00fcller","year":"1830"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb447","doi-asserted-by":"crossref","first-page":"1073","DOI":"10.1007\/s00467-010-1454-9","article-title":"HNF1B alterations associated with congenital anomalies of the kidney and urinary tract","volume":"25","author":"Nakayama","year":"2010","journal-title":"The Journal of Pediatric Nephrology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0285","series-title":"Developmental stages in human embryos: Including a revision of Streeter's \"Horizons\" and a survey of the Carnegie collection","author":"O'Rahilly","year":"1987"},{"issue":"364","key":"10.1016\/bs.ctdb.2021.12.004_bb0290","first-page":"e361","article-title":"Mutations in the hepatocyte nuclear factor-1beta (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations","volume":"203","author":"Oram","year":"2010","journal-title":"American Journal of Obstetrics and Gynecology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0295","doi-asserted-by":"crossref","first-page":"657","DOI":"10.1007\/s00247-007-0497-y","article-title":"Herlyn-Werner-Wunderlich syndrome: Uterus didelphys, blind hemivagina and ipsilateral renal agenesis. Sonographic and MR findings in 11 cases","volume":"37","author":"Orazi","year":"2007","journal-title":"Pediatric Radiology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb446","series-title":"Developmental stages in human embryos","author":"O\u2019Rahilly","year":"1987"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0300","doi-asserted-by":"crossref","first-page":"493","DOI":"10.1016\/j.ydbio.2007.03.027","article-title":"Cellular mechanisms of Mullerian duct formation in the mouse","volume":"306","author":"Orvis","year":"2007","journal-title":"Developmental Biology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0305","doi-asserted-by":"crossref","first-page":"350","DOI":"10.1038\/374350a0","article-title":"Dorsalizing signal Wnt-7a required for normal polarity of D-V and A-P axes of mouse limb","volume":"374","author":"Parr","year":"1995","journal-title":"Nature"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0310","doi-asserted-by":"crossref","first-page":"707","DOI":"10.1038\/27221","article-title":"Sexually dimorphic development of the mammalian reproductive tract requires Wnt-7a","volume":"395","author":"Parr","year":"1998","journal-title":"Nature"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0315","series-title":"Embryology of the pig","author":"Patten","year":"1948"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0320","first-page":"1013","article-title":"Reconstruction du pelvis d'un embryon humain de 7, 5mm (stade XVI de Streeter)","volume":"52","author":"Pillet","year":"1967","journal-title":"Comptes rendus de l\u2019Association des anatomistes"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0325","doi-asserted-by":"crossref","first-page":"643","DOI":"10.1111\/j.1471-0528.1922.tb16100.x","article-title":"A case of unilateral H\u00e6matokolpos, H\u00e6matometra and H\u00e6matosalpinx","volume":"29","author":"Purslow","year":"1922","journal-title":"BJOG: An International Journal of Obstetrics & Gynaecology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0330","first-page":"899","article-title":"Clinical diagnosis of uterine didelphia in Ayrshire heifer","volume":"47","author":"Raggio","year":"2006","journal-title":"The Canadian Veterinary Journal"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0335","doi-asserted-by":"crossref","first-page":"371","DOI":"10.1007\/s00429-002-0267-4","article-title":"An ultrastructural study of interstitial implantation in captive-bred, short-tailed fruit bats, Carollia perspicillata: Trophoblastic adhesion and penetration of the uterine epithelium","volume":"205","author":"Rasweiler","year":"2002","journal-title":"Anatomy and Embryology (Berlin)"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0340","series-title":"Mammal phylogeny","first-page":"4","article-title":"Ontogeny, genetic control, and phylogeny of female reproduction in monotreme and therian mammals","author":"Renfree","year":"1993"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0345","doi-asserted-by":"crossref","first-page":"3549","DOI":"10.1111\/j.1742-4658.2012.08729.x","article-title":"The PDZ protein discs-large (DLG): The 'Jekyll and Hyde' of the epithelial polarity proteins","volume":"279","author":"Roberts","year":"2012","journal-title":"The FEBS Journal"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0350","series-title":"A comparative overview of mammalian fertilization","first-page":"117","article-title":"Fertilization of marsupials","author":"Rodger","year":"1991"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0355","doi-asserted-by":"crossref","first-page":"789","DOI":"10.1016\/j.ajhg.2017.09.018","article-title":"Exome-wide association study identifies GREB1L mutations in congenital kidney malformations","volume":"101","author":"Sanna-Cherchi","year":"2017","journal-title":"American Journal of Human Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0360","doi-asserted-by":"crossref","first-page":"415","DOI":"10.1093\/humupd\/dmn018","article-title":"Prevalence and diagnosis of congenital uterine anomalies in women with reproductive failure: A critical appraisal","volume":"14","author":"Saravelos","year":"2008","journal-title":"Human Reproduction Update"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0365","doi-asserted-by":"crossref","first-page":"566","DOI":"10.1111\/ahe.12398","article-title":"Morphology of the vaginal complex in the white-eared opossum (Didelphis albiventris): Gross anatomy and light microscopy","volume":"47","author":"Schimming","year":"2018","journal-title":"Anatomia, Histologia, Embryologia"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0370","doi-asserted-by":"crossref","first-page":"459","DOI":"10.1007\/s00439-018-1898-8","article-title":"De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness","volume":"137","author":"Schrauwen","year":"2018","journal-title":"Human Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0375","doi-asserted-by":"crossref","DOI":"10.3390\/genes11060687","article-title":"Autosomal dominantly inherited GREB1L variants in individuals with profound sensorineural hearing impairment","volume":"11","author":"Schrauwen","year":"2020","journal-title":"Genes (Basel)"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0380","doi-asserted-by":"crossref","first-page":"425","DOI":"10.1038\/374425a0","article-title":"Requirement for Lim1 in head-organizer function","volume":"374","author":"Shawlot","year":"1995","journal-title":"Nature"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0385","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1016\/S0070-2153(05)68004-0","article-title":"Comparative developmental biology of the mammalian uterus","volume":"68","author":"Spencer","year":"2005","journal-title":"Current Topics in Developmental Biology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0390","doi-asserted-by":"crossref","first-page":"679","DOI":"10.1038\/372679a0","article-title":"Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4","volume":"372","author":"Stark","year":"1994","journal-title":"Nature"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb459","doi-asserted-by":"crossref","unstructured":"Stern A.M., Gall Jr J.C., Perry B. L., Stimson C.W., 1969. Hand-foot-uterus syndrome, Lancet 1 (7594), 577, doi: 10.1016\/s0140-6736(69)91994-1. PMID: 4179869","DOI":"10.1016\/S0140-6736(69)91994-1"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0395","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1136\/vr.151.7.217","article-title":"Uterus didelphys in a goat","volume":"151","author":"Timurkaan","year":"2002","journal-title":"The Veterinary Record"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0400","doi-asserted-by":"crossref","first-page":"4057","DOI":"10.1242\/dev.121.12.4057","article-title":"Pax-2 controls multiple steps of urogenital development","volume":"121","author":"Torres","year":"1995","journal-title":"Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0405","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1038\/17068","article-title":"Female development in mammals is regulated by Wnt-4 signalling","volume":"397","author":"Vainio","year":"1999","journal-title":"Nature"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0410","doi-asserted-by":"crossref","first-page":"111","DOI":"10.1159\/000046185","article-title":"Ultrastructural changes in the uterine luminal and glandular epithelium during the oestrous cycle of the marsupial Monodelphis domestica (grey short-tailed opossum)","volume":"170","author":"Wick","year":"2002","journal-title":"Cells, Tissues, Organs"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0415","doi-asserted-by":"crossref","first-page":"19272","DOI":"10.1073\/pnas.1013226107","article-title":"Uterine epithelial estrogen receptor alpha is dispensable for proliferation but essential for complete biological and biochemical responses","volume":"107","author":"Winuthayanon","year":"2010","journal-title":"Proceedings of the National Academy of Sciences of the United States of America"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0420","doi-asserted-by":"crossref","first-page":"451","DOI":"10.1016\/0092-8674(81)90009-X","article-title":"The discs-large tumor suppressor gene of Drosophila encodes a guanylate kinase homolog localized at septate junctions","volume":"66","author":"Woods","year":"1991","journal-title":"Cell"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0430","doi-asserted-by":"crossref","first-page":"402","DOI":"10.1086\/506332","article-title":"Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi\/Raas-Rothschild\/Schinzel phocomelia syndrome","volume":"79","author":"Woods","year":"2006","journal-title":"American Journal of Human Genetics"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0425","doi-asserted-by":"crossref","first-page":"1469","DOI":"10.1083\/jcb.134.6.1469","article-title":"Dlg protein is required for junction structure, cell polarity, and proliferation control in Drosophila epithelia","volume":"134","author":"Woods","year":"1996","journal-title":"The Journal of Cell Biology"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0435","doi-asserted-by":"crossref","first-page":"1211","DOI":"10.1242\/dev.126.6.1211","article-title":"A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo","volume":"126","author":"Yamaguchi","year":"1999","journal-title":"Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0440","doi-asserted-by":"crossref","first-page":"5301","DOI":"10.1242\/dev.129.22.5301","article-title":"Sonic hedgehog regulates proliferation and differentiation of mesenchymal cells in the mouse metanephric kidney","volume":"129","author":"Yu","year":"2002","journal-title":"Development"},{"key":"10.1016\/bs.ctdb.2021.12.004_bb0445","doi-asserted-by":"crossref","first-page":"23037","DOI":"10.1038\/srep23037","article-title":"Novel function of LHFPL2 in female and male distal reproductive tract development","volume":"6","author":"Zhao","year":"2016","journal-title":"Scientific Reports"}],"container-title":["Current Topics in Developmental Biology","Mouse Models of Development and Disease"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0070215321000946?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0070215321000946?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2023,1,3]],"date-time":"2023-01-03T08:09:40Z","timestamp":1672733380000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0070215321000946"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022]]},"ISBN":["9780128171318"],"references-count":107,"URL":"https:\/\/doi.org\/10.1016\/bs.ctdb.2021.12.004","relation":{},"ISSN":["0070-2153"],"issn-type":[{"value":"0070-2153","type":"print"}],"subject":[],"published":{"date-parts":[[2022]]}}}