{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,14]],"date-time":"2026-11-14T08:00:54Z","timestamp":1794643254636,"version":"4.9.1"},"reference-count":34,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2015,9,1]],"date-time":"2015-09-01T00:00:00Z","timestamp":1441065600000},"content-version":"tdm","delay-in-days":1699,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2011,2]]},"DOI":"10.1111\/j.1399-0004.2010.01443.x","type":"journal-article","created":{"date-parts":[[2010,4,8]],"date-time":"2010-04-08T18:07:19Z","timestamp":1270750039000},"page":"169-175","source":"Crossref","is-referenced-by-count":30,"title":["The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders"],"prefix":"10.1111","volume":"79","author":[{"given":"DK","family":"Bourque","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"MS","family":"Pe\u00f1aherrera","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"RKC","family":"Yuen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"MI","family":"Van Allen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"DE","family":"McFadden","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"WP","family":"Robinson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2011,1,6]]},"reference":[{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB1|cit1","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1080\/15513810802545350","article-title":"Immunohistochemical expression of p57 in placental vascular proliferative disorders of preterm and term placentas","volume":"28","author":"Allias","year":"2009","journal-title":"Fetal Pediatr Pathol"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB2|cit2","doi-asserted-by":"crossref","first-page":"633","DOI":"10.1038\/268633a0","article-title":"Androgenetic origin of hydatidiform mole","volume":"268","author":"Kajii","year":"1977","journal-title":"Nature"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB3|cit3","doi-asserted-by":"crossref","first-page":"19","DOI":"10.1002\/0470846666.ch3","article-title":"Imprinted genes and the coordination of fetal and postnatal growth in mammals","volume":"237","author":"Reik","year":"2001","journal-title":"Novartis Found Symp"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB4|cit4","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1002\/ajmg.c.30058","article-title":"Beckwith-Wiedemann syndrome","volume":"137","author":"Weksberg","year":"2005","journal-title":"Am J Med Genet C Semin Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB5|cit5","first-page":"347","article-title":"Methylation profiling in individuals with Silver-Russell Syndrome","volume":"152A","author":"Pe\u00f1aherrera","year":"2010","journal-title":"Am J Hum Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB6|cit6","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1136\/jmg.2006.044370","article-title":"The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome","volume":"44","author":"Schonherr","year":"2007","journal-title":"J Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB7|cit7","doi-asserted-by":"crossref","first-page":"194","DOI":"10.1016\/S0168-9525(98)01432-2","article-title":"Imprinting in Prader-Willi and Angelman syndromes","volume":"14","author":"Nicholls","year":"1998","journal-title":"Trends Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB8|cit8","doi-asserted-by":"crossref","first-page":"313","DOI":"10.1007\/BF00220089","article-title":"Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13","volume":"90","author":"Dittrich","year":"1992","journal-title":"Hum Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB9|cit9","doi-asserted-by":"crossref","first-page":"732","DOI":"10.1007\/s10024-005-0061-4","article-title":"Partly molar pregnancies that are not partial moles: additional possibilities and implications","volume":"8","author":"Sebire","year":"2005","journal-title":"Pediatr Dev Pathol"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB10|cit10","doi-asserted-by":"crossref","first-page":"725","DOI":"10.1111\/j.1471-0528.2006.00929.x","article-title":"Heterogeneity in the origin of recurrent complete hydatidiform moles: not all women with multiple molar pregnancies have biparental moles","volume":"113","author":"van der Smagt","year":"2006","journal-title":"Br J Obstet Gynecol"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB11|cit11","doi-asserted-by":"crossref","first-page":"805","DOI":"10.1097\/PAS.0b013e318191f309","article-title":"Diagnosis and subclassification of hydatidiform moles using p57 immunohistochemistry and molecular genotyping: validation and prospective analysis in routine and consultation practice settings with development of an algorithmic approach","volume":"33","author":"McConnell","year":"2009","journal-title":"Am J Surg Pathol"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB12|cit12","doi-asserted-by":"crossref","first-page":"300","DOI":"10.1038\/ng1740","article-title":"Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans","volume":"38","author":"Murdoch","year":"2006","journal-title":"Nat Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB13|cit13","doi-asserted-by":"crossref","first-page":"569","DOI":"10.1136\/jmg.2008.064196","article-title":"Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region","volume":"46","author":"Wang","year":"2009","journal-title":"J Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB14|cit14","doi-asserted-by":"crossref","first-page":"8064","DOI":"10.1073\/pnas.96.14.8064","article-title":"A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome","volume":"96","author":"Smilinich","year":"1999","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB15|cit15","doi-asserted-by":"crossref","first-page":"288","DOI":"10.1016\/j.ygeno.2004.03.008","article-title":"The KCNQ1OT1 promoter, a key regulator of genomic imprinting in human chromosome 11p15.5.","volume":"84","author":"Du","year":"2004","journal-title":"Genomics"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB16|cit16","doi-asserted-by":"crossref","first-page":"797","DOI":"10.1136\/jmg.40.11.797","article-title":"Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome","volume":"40","author":"Diaz-Meyer","year":"2003","journal-title":"J Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB17|cit17","doi-asserted-by":"crossref","first-page":"3267","DOI":"10.1093\/hmg\/11.26.3267","article-title":"The maternally transcribed gene p57(KIP2) (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles","volume":"11","author":"Fisher","year":"2002","journal-title":"Hum Mol Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB18|cit18","doi-asserted-by":"crossref","first-page":"1155","DOI":"10.1038\/modpathol.3800175","article-title":"Complete hydatidiform mole retaining a chromosome 11 of maternal origin: molecular genetic analysis of a case","volume":"17","author":"Fisher","year":"2004","journal-title":"Mod Pathol"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB19|cit19","doi-asserted-by":"crossref","first-page":"1114","DOI":"10.1093\/humrep\/del462","article-title":"Origin and outcome of pregnancies affected by androgenetic\/biparental chimerism","volume":"22","author":"Robinson","year":"2007","journal-title":"Hum Reprod"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB20|cit20","doi-asserted-by":"crossref","first-page":"1752","DOI":"10.1002\/ajmg.a.31800","article-title":"Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5.","volume":"143","author":"Robinson","year":"2007","journal-title":"Am J Med Genet A"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB21|cit21","doi-asserted-by":"crossref","first-page":"447","DOI":"10.1046\/j.1365-2559.2001.01256.x","article-title":"Pseudo-partial moles: placental stem vessel hydrops and the association with Beckwith-Wiedemann syndrome and complete moles","volume":"39","author":"Paradinas","year":"2001","journal-title":"Histopathology"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB22|cit22","doi-asserted-by":"crossref","first-page":"535","DOI":"10.1002\/ajmg.1320380407","article-title":"Two different phenotypes of fetuses with chromosomal triploidy: correlation with parental origin of the extra haploid set","volume":"38","author":"McFadden","year":"1991","journal-title":"Am J Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB23|cit23","doi-asserted-by":"crossref","first-page":"192","DOI":"10.1034\/j.1399-0004.2000.580306.x","article-title":"Parental and meiotic origin of triploidy in the fetal and embryonic period","volume":"58","author":"McFadden","year":"2000","journal-title":"Clin Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB24|cit24","doi-asserted-by":"crossref","first-page":"3727","DOI":"10.1242\/dev.01241","article-title":"Selective loss of imprinting in the placenta following preimplantation development in culture","volume":"131","author":"Mann","year":"2004","journal-title":"Development"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB25|cit25","doi-asserted-by":"crossref","first-page":"1291","DOI":"10.1038\/ng1468","article-title":"Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation","volume":"36","author":"Lewis","year":"2004","journal-title":"Nat Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB26|cit26","doi-asserted-by":"crossref","first-page":"6623","DOI":"10.1073\/pnas.0511031103","article-title":"Limited evolutionary conservation of imprinting in the human placenta","volume":"103","author":"Monk","year":"2006","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB27|cit27","doi-asserted-by":"crossref","first-page":"3037","DOI":"10.1093\/humrep\/17.12.3037","article-title":"Dispermy-origin of diandric triploidy: brief communication","volume":"17","author":"McFadden","year":"2002","journal-title":"Hum Reprod"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB28|cit28","doi-asserted-by":"crossref","first-page":"609","DOI":"10.1136\/jmg.2005.037747","article-title":"Phenotype of triploid embryos","volume":"43","author":"McFadden","year":"2006","journal-title":"J Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB29|cit29","doi-asserted-by":"crossref","first-page":"2989","DOI":"10.1093\/hmg\/10.26.2989","article-title":"Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1","volume":"10","author":"Weksberg","year":"2001","journal-title":"Hum Mol Genet"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB30|cit30","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1016\/j.placenta.2009.12.003","article-title":"Decreased placental methylation at the H19\/IGF2 imprinting control region is associated with normotensive intrauterine growth restriction but not preeclampsia","volume":"31","author":"Bourque","year":"2010","journal-title":"Placenta"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB31|cit31","doi-asserted-by":"crossref","first-page":"48","DOI":"10.2144\/000112312","article-title":"Optimizing annealing temperature overcomes bias in bisulfite PCR methylation analysis","volume":"42","author":"Shen","year":"2007","journal-title":"Biotechniques"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB32|cit32","doi-asserted-by":"crossref","first-page":"14857","DOI":"10.1073\/pnas.95.25.14857","article-title":"A model system to study genomic imprinting of human genes","volume":"95","author":"Gabriel","year":"1998","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB33|cit33","doi-asserted-by":"crossref","first-page":"2415","DOI":"10.1002\/ajmg.a.33065","article-title":"Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell-Silver syndrome","volume":"149A","author":"Horike","year":"2009","journal-title":"Am J Med Genet A"},{"key":"10.1111\/j.1399-0004.2010.01443.x-BIB34|cit34","doi-asserted-by":"crossref","first-page":"2023","DOI":"10.1371\/journal.pgen.0030181","article-title":"Genome-wide profiling of DNA methylation reveals a class of normally methylated CpG island promoters","volume":"3","author":"Shen","year":"2007","journal-title":"PLoS Genet"}],"container-title":["Clinical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fj.1399-0004.2010.01443.x","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1111\/j.1399-0004.2010.01443.x\/fullpdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,3,25]],"date-time":"2024-03-25T17:10:18Z","timestamp":1711386618000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/j.1399-0004.2010.01443.x"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,1,6]]},"references-count":34,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2011,2]]}},"URL":"https:\/\/doi.org\/10.1111\/j.1399-0004.2010.01443.x","relation":{},"ISSN":["0009-9163"],"issn-type":[{"value":"0009-9163","type":"print"}],"subject":[],"published":{"date-parts":[[2011,1,6]]}}}