{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,11]],"date-time":"2026-09-11T02:27:35Z","timestamp":1789093655727,"version":"build-2803163510"},"reference-count":70,"publisher":"Public Library of Science (PLoS)","issue":"2","license":[{"start":{"date-parts":[[2017,2,7]],"date-time":"2017-02-07T00:00:00Z","timestamp":1486425600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/publicdomain\/zero\/1.0\/"}],"content-domain":{"domain":["www.plosone.org"],"crossmark-restriction":false},"short-container-title":["PLoS ONE"],"DOI":"10.1371\/journal.pone.0171449","type":"journal-article","created":{"date-parts":[[2017,2,7]],"date-time":"2017-02-07T18:39:49Z","timestamp":1486492789000},"page":"e0171449","update-policy":"https:\/\/doi.org\/10.1371\/journal.pone.corrections_policy","source":"Crossref","is-referenced-by-count":5,"title":["Cellular and ultrastructural characterization of the grey-morph phenotype in southern right whales (Eubalaena australis)"],"prefix":"10.1371","volume":"12","author":[{"given":"Guy D.","family":"Eroh","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fred C.","family":"Clayton","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Scott R.","family":"Florell","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pamela B.","family":"Cassidy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrea","family":"Chirife","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carina F.","family":"Mar\u00f3n","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Luciano O.","family":"Valenzuela","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael S.","family":"Campbell","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jon","family":"Seger","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Victoria J.","family":"Rowntree","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sancy A.","family":"Leachman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"340","published-online":{"date-parts":[[2017,2,7]]},"reference":[{"key":"ref1","first-page":"161","article-title":"Dictionaire classique d'Histoire naturelle","volume":"2","author":"A. Desmoulins","year":"1822"},{"key":"ref2","first-page":"114","article-title":"Natural markings and their use in determining calving intervals in right whales off South America. S. Afr","volume":"25","author":"P.B. Best","year":"1990","journal-title":"Journal of Zoology"},{"key":"ref3","first-page":"371","article-title":"Report of the International Whaling Commission, Special Issue Selected Symposium 76, Whales","author":"R Payne","year":"1983"},{"issue":"11","key":"ref4","doi-asserted-by":"crossref","first-page":"3439","DOI":"10.1111\/j.1365-294X.2005.02664.x","article-title":"Population histories of right whales (Cetacea: Eubalaena) inferred from mitochondrial sequence diversities and divergences of their whale lice (Amphipoda: Cyamus)","volume":"14","author":"ZA Kaliszewska","year":"2005","journal-title":"Mol Ecol. Oct"},{"issue":"Special Issue 10","key":"ref5","first-page":"161","article-title":"Long Term Behavioral Studies of the Southern Right Whale (Eubalaena Australis)","author":"R Payne","year":"1986","journal-title":"Rep. Int. Whal. Commn"},{"issue":"4","key":"ref6","doi-asserted-by":"crossref","first-page":"464","DOI":"10.1093\/jhered\/90.4.464","article-title":"Dorsal Skin Color Patterns among Southern Right Whales (Eubalaena Australis): Genetic Basis and Evolutionary Significance","volume":"90","author":"CM Schaeff","year":"1999","journal-title":"Journal of Heredity"},{"issue":"6","key":"ref7","doi-asserted-by":"crossref","first-page":"530","DOI":"10.1002\/bies.20767","article-title":"The origin and evolution of the neural crest","volume":"30","author":"PCJ Donoghue","year":"2008","journal-title":"Bioessays"},{"issue":"Issue 3","key":"ref8","doi-asserted-by":"crossref","first-page":"701","DOI":"10.1111\/j.1748-7692.1999.tb00837.x","article-title":"Genetic basis and evolutionary significance of ventral skin color markings in north Atlantic right whales (Eubalena glacialis)","volume":"Volume 15","author":"CM Schaeff","year":"1999","journal-title":"Marine Mammal Science"},{"issue":"4581","key":"ref9","doi-asserted-by":"crossref","first-page":"326","DOI":"10.1038\/180326a0","article-title":"Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin","volume":"180","author":"VM Ingram","year":"1957","journal-title":"Nature"},{"issue":"11","key":"ref10","doi-asserted-by":"crossref","first-page":"499","DOI":"10.1073\/pnas.27.11.499","article-title":"Genetic control of biochemical reactions in Neurospora","volume":"27","author":"GW Beadle","year":"1941","journal-title":"Proc Natl Acad Sci U S A"},{"issue":"3","key":"ref11","doi-asserted-by":"crossref","first-page":"379","DOI":"10.1002\/wdev.72","article-title":"The etiology and molecular genetics of human pigmentation disorders","volume":"2","author":"LL Baxter","year":"2013","journal-title":"Wiley Interdiscip Rev Dev Biol"},{"issue":"4","key":"ref12","doi-asserted-by":"crossref","first-page":"459","DOI":"10.1016\/j.cub.2014.01.020","article-title":"Epistatic and combinatorial effects of pigmentary gene mutations in the domestic pigeon","volume":"24","author":"ET Domyan","year":"2014","journal-title":"Current Biology"},{"key":"ref13","doi-asserted-by":"crossref","first-page":"411","DOI":"10.1111\/j.1755-148X.2012.01014.x","article-title":"Unraveling the thread of nature\u2019s tapestry: the genetics of diversity and convergence in animal pigmentation","volume":"25","author":"MR Kronforst","year":"2012","journal-title":"Pigment Cell Melanoma Res"},{"issue":"5919","key":"ref14","doi-asserted-by":"crossref","first-page":"1339","DOI":"10.1126\/science.1165448","article-title":"Molecular and Evolutionary History of melanism in North American gray wolves","volume":"323","author":"TM Anderson","year":"2009","journal-title":"Science"},{"key":"ref15","doi-asserted-by":"crossref","first-page":"4392","DOI":"10.1073\/pnas.85.12.4392","article-title":"A cDNA encoding tyrosinase-related protein maps to the brown locus in mouse","volume":"Vol. 85","author":"IJ Jackson","year":"1988","journal-title":"Proc. Nati. Acad. Sci. USA"},{"issue":"5","key":"ref16","doi-asserted-by":"crossref","first-page":"322","DOI":"10.1111\/j.1600-0749.2005.00269.x","article-title":"The Silver locus product Pmel17\/gp100\/Silv\/ME20: controversial in name and in function","volume":"18","author":"AC Theos","year":"2005","journal-title":"Pigment Cell Res"},{"issue":"4","key":"ref17","doi-asserted-by":"crossref","first-page":"333","DOI":"10.1034\/j.1600-0749.2003.00067.x","article-title":"The color loci of mice\u2014a genetic century","volume":"16","author":"DC Bennett","year":"2003","journal-title":"Pigment Cell Res"},{"key":"ref18","doi-asserted-by":"crossref","first-page":"576","DOI":"10.1016\/j.semcdb.2013.03.014","article-title":"Pleiotropic effects of coat colour-associated mutations in humans, mice and other mammals","volume":"24","author":"M Reissmann","year":"2013","journal-title":"Seminars in Cell & Developmental Biology"},{"key":"ref19","first-page":"407","article-title":"Albinism, partial albinism, and vitiligo","volume":"33","author":"TP Kugelman","year":"1961","journal-title":"Yale J Biol Med"},{"key":"ref20","doi-asserted-by":"crossref","first-page":"28","DOI":"10.1038\/jid.1965.87","article-title":"Electron microscopy of melanocytes in human piebaldism","volume":"45","author":"AS Breathnach","year":"1965","journal-title":"J Invest Dermatol"},{"key":"ref21","doi-asserted-by":"crossref","first-page":"392","DOI":"10.1016\/0012-1606(71)90088-1","article-title":"The ultrastructural effects of the \/ and s loci upon black-red melanin differentiation in the fowl","volume":"24","author":"JA Brumbauch","year":"1971","journal-title":"Developmental Biology"},{"key":"ref22","doi-asserted-by":"crossref","first-page":"132","DOI":"10.1046\/j.1365-2141.2003.04557.x","article-title":"Molecular, ultrastructural and functional characterization of a Spanish family with Hermansky\u2014Pudlak syndrome: role of insC974 in platelet function and clinical relevance","volume":"123","author":"R Gonz\u00e1lez-Conejero","year":"2003","journal-title":"British Journal of Haematology"},{"issue":"4","key":"ref23","doi-asserted-by":"crossref","first-page":"620","DOI":"10.1242\/dev.106567","article-title":"The melanocyte lineage in development and disease","volume":"142","author":"RL Mort","year":"2015","journal-title":"Development"},{"issue":"3","key":"ref24","doi-asserted-by":"crossref","first-page":"316","DOI":"10.1111\/pcmr.12080","article-title":"Cellular and molecular mechanisms controlling the migration of melanocytes and melanoma cells","volume":"26","author":"J Bonaventure","year":"2013","journal-title":"Pigment Cell Melanoma Res"},{"key":"ref25","doi-asserted-by":"crossref","first-page":"baq025","DOI":"10.1093\/database\/baq025","article-title":"A curated online resource for SOX10 and pigment cell molecular genetic pathways","volume":"2010","author":"LL Baxter","year":"2010","journal-title":"Database"},{"key":"ref26","doi-asserted-by":"crossref","first-page":"365","DOI":"10.1146\/annurev.genet.38.072902.092717","article-title":"Melanocytes and the microphthalmia transcription factor network","volume":"38","author":"E Steingr\u00edmsson","year":"2004","journal-title":"Annu. Rev. Genet"},{"key":"ref27","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/s004390000328","article-title":"Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3","volume":"107","author":"SB Potterf","year":"2000","journal-title":"Hum. Genet"},{"key":"ref28","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1034\/j.1600-0749.2002.01080.x","article-title":"Identification of a distal enhancer for the melanocyte-specific promoter of the MITF gene","volume":"15","author":"K Watanabe","year":"2002","journal-title":"Pigment Cell Res"},{"key":"ref29","doi-asserted-by":"crossref","first-page":"1907","DOI":"10.1093\/hmg\/9.13.1907","article-title":"Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome","volume":"9","author":"N Bondurand","year":"2000","journal-title":"Hum. Mol. Genet"},{"key":"ref30","doi-asserted-by":"crossref","first-page":"1467","DOI":"10.1242\/dev.128.8.1467","article-title":"The winged-helix transcription factor FoxD3 is important for establishing the neural crest lineage and repressing melanogenesis in avian embryos","volume":"128","author":"R Kos","year":"2001","journal-title":"Development"},{"key":"ref31","doi-asserted-by":"crossref","first-page":"2269","DOI":"10.1242\/dev.093294","article-title":"A dynamic code of dorsal neural tube genes regulates the segregation between neurogenic and melanogenic neural crest cells","volume":"140","author":"E Nitzan","year":"2013","journal-title":"Development"},{"key":"ref32","doi-asserted-by":"crossref","first-page":"12709","DOI":"10.1073\/pnas.1306287110","article-title":"Neural crest and Schwann cell progenitor-derived melanocytes are two spatially segregated populations similarly regulated by Foxd3","volume":"110","author":"E Nitzan","year":"2013","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"ref33","doi-asserted-by":"crossref","first-page":"461","DOI":"10.1016\/j.ydbio.2013.12.010","article-title":"Pax3 and Zic1 trigger the early neural crest gene regulatory network by the direct activation of multiple key neural crest specifiers","volume":"386","author":"JL Plouhinec","year":"2014","journal-title":"Dev. Biol"},{"key":"ref34","doi-asserted-by":"crossref","first-page":"22","DOI":"10.1006\/dbio.2001.0222","article-title":"Wnt and BMP signalling govern lineage segregation of melanocytes in the avian embryo","volume":"233","author":"EJ Jin","year":"2001","journal-title":"Dev. Biol"},{"key":"ref35","doi-asserted-by":"crossref","first-page":"14013","DOI":"10.1074\/jbc.C000113200","article-title":"Induction of melanocyte-specific microphthalmia-associated transcription factor by Wnt-3a","volume":"275","author":"K Takeda","year":"2000","journal-title":"J. Biol. Chem"},{"key":"ref36","doi-asserted-by":"crossref","first-page":"596","DOI":"10.1002\/ar.20535","article-title":"Structure of the integument of southern right whales, Eubalaena australis","volume":"290","author":"D Reeb","year":"2007","journal-title":"The Anatomical Record"},{"issue":"2","key":"ref37","first-page":"277","article-title":"Epidermal ultrastructure of the southern right whale calf (Eubalaena australis)","volume":"28","author":"CJ Pfeiffer","year":"1996","journal-title":"J Submicrosc Cytol Pathol"},{"key":"ref38","doi-asserted-by":"crossref","first-page":"721","DOI":"10.1139\/z99-249","article-title":"Stable-isotope and electron-microscopic evidence that cyamids (Crustacea: Amphipoda) feed on whale skin","volume":"78","author":"DM Schell","year":"2000","journal-title":"Can. J. Zool"},{"key":"ref39","doi-asserted-by":"crossref","first-page":"2386","DOI":"10.1038\/srep02386","article-title":"Whales use distinct strategies to counteract solar ultraviolet radiation","volume":"3","author":"LM Martinez-Levasseur","year":"2013","journal-title":"Scientific Reports"},{"key":"ref40","doi-asserted-by":"crossref","first-page":"17","DOI":"10.3354\/dao02986","article-title":"Post-mortem findings in southern right whales Eubalaena australis at Pen\u00ednsula Vald\u00e9s, Argentina, 2003\u20132012","volume":"119","author":"D McAloose","year":"2016","journal-title":"Dis Aquat Org"},{"key":"ref41","unstructured":"Sironi M, Rowntree VJ, Di Martino M, Chirife A, Bandieri L, Beltramino L et al. 2012. Southern right whale mortalities at Pen\u00ednsula Vald\u00e9s, Argentina: updated information for 2010\u20132011. SC\/64\/BRG12 presented to the International Whaling Commission Scientific Committee, Panama (unpublished). [Available from the IWC Office]."},{"issue":"2","key":"ref42","doi-asserted-by":"crossref","first-page":"116","DOI":"10.1038\/modpathol.3880267","article-title":"Preservation of RNA for functional genomic studies: a multidisciplinary tumor bank protocol","volume":"14","author":"SR Florell","year":"2001","journal-title":"Mod Pathol"},{"issue":"4","key":"ref43","doi-asserted-by":"crossref","first-page":"1155","DOI":"10.1152\/physrev.00044.2003","article-title":"Melanin pigmentation in mammalian skin and its hormonal regulation","volume":"84","author":"A Slominski","year":"2004","journal-title":"Physiol Rev"},{"issue":"No. 641","key":"ref44","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1098\/rstb.1952.0012","article-title":"The Chemical Basis of Morphogenesis","volume":"Vol. 237","author":"AM Turing","year":"1952","journal-title":"Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences"},{"issue":"12","key":"ref45","doi-asserted-by":"crossref","first-page":"4397","DOI":"10.1073\/pnas.1322005111","article-title":"Testing Turing\u2019s theory of morphogenesis in chemical cells","volume":"111","author":"N Tompkins","year":"2014","journal-title":"Proc Natl Acad Sci USA"},{"issue":"19","key":"ref46","doi-asserted-by":"crossref","first-page":"8696","DOI":"10.1073\/pnas.88.19.8696","article-title":"Mutation of the KIT (mast\/stem cell growth factor receptor) protooncogene in human piebaldism","volume":"88","author":"LB Giebel","year":"1991","journal-title":"Proc Natl Acad Sci U S A"},{"issue":"7","key":"ref47","doi-asserted-by":"crossref","first-page":"519","DOI":"10.1001\/jama.1966.03100070063019","article-title":"Partial albinism","volume":"195","author":"DE Comings","year":"1966","journal-title":"JAMA"},{"issue":"3","key":"ref48","doi-asserted-by":"crossref","first-page":"676","DOI":"10.1038\/sj.jid.5700639","article-title":"Piebald trait: implication of kit mutation on in vitro melanocyte survival and on the clinical application of cultured epidermal autografts","volume":"127","author":"S Bondanza","year":"2007","journal-title":"J Invest Dermatol"},{"key":"ref49","article-title":"Driver KIT mutations in melanoma cluster in four hotspots","author":"N Dumaz","year":"2014","journal-title":"Melanoma Res"},{"issue":"6","key":"ref50","doi-asserted-by":"crossref","first-page":"1182","DOI":"10.1038\/jid.2011.67","article-title":"The genetic determination of skin pigmentation: KITLG and the KITLG\/c-Kit pathway as key players in the onset of human familial pigmentary diseases","volume":"131","author":"M Picardo","year":"2011","journal-title":"J Invest Dermatol"},{"issue":"2","key":"ref51","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1002\/ajmg.a.20345","article-title":"Deletion of the SLUG (SNAI2) gene results in human piebaldism","volume":"122A","author":"M S\u00e1nchez-Mart\u00edn","year":"2003","journal-title":"Am J Med Genet A"},{"issue":"50","key":"ref52","doi-asserted-by":"crossref","first-page":"18081","DOI":"10.1073\/pnas.0506216102","article-title":"MicroRNAs 221 and 222 inhibit normal erythropoiesis and erythroleukemic cell growth via kit receptor down-modulation","volume":"102","author":"N Felli","year":"2005","journal-title":"Proc Natl Acad Sci U S A"},{"issue":"2","key":"ref53","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1002\/ajmg.1320580205","article-title":"Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature","volume":"58","author":"CT Baldwin","year":"1995","journal-title":"Am J Med Genet"},{"issue":"1","key":"ref54","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1002\/ajmg.1320400113","article-title":"Waardenburg I syndrome: a clinical and genetic study of two large Brazilian kindreds, and literature review","volume":"40","author":"EO da-Silva","year":"1991","journal-title":"Am J Med Genet"},{"issue":"3","key":"ref55","first-page":"455","article-title":"Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)","volume":"52","author":"CF Hoth","year":"1993","journal-title":"Am J Hum Genet"},{"issue":"1","key":"ref56","doi-asserted-by":"crossref","first-page":"26","DOI":"10.1038\/ng0193-26","article-title":"Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2","volume":"3","author":"M Tassabehji","year":"1993","journal-title":"Nat Genet"},{"issue":"4","key":"ref57","doi-asserted-by":"crossref","first-page":"703","DOI":"10.1093\/hmg\/7.4.703","article-title":"Mutation at the anophthalmic white locus in Syrian hamsters: haploinsufficiency in the Mitf gene mimics human Waardenburg syndrome type 2","volume":"7","author":"CA Hodgkinson","year":"1998","journal-title":"Hum Mol Genet"},{"issue":"3","key":"ref58","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1038\/ng1194-251","article-title":"Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene","volume":"8","author":"M Tassabehji","year":"1994","journal-title":"Nat Genet"},{"issue":"6","key":"ref59","doi-asserted-by":"crossref","first-page":"1169","DOI":"10.1086\/522090","article-title":"Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4","volume":"81","author":"N Bondurand","year":"2007","journal-title":"Am J Hum Genet"},{"issue":"2","key":"ref60","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1038\/ng0298-171","article-title":"SOX10 mutations in patients with Waardenburg-Hirschsprung disease","volume":"18","author":"V Pingault","year":"1998","journal-title":"Nat Genet"},{"issue":"36","key":"ref61","doi-asserted-by":"crossref","first-page":"23033","DOI":"10.1074\/jbc.273.36.23033","article-title":"Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients","volume":"273","author":"K Kuhlbrodt","year":"1998","journal-title":"J Biol Chem"},{"issue":"25","key":"ref62","doi-asserted-by":"crossref","first-page":"3231","DOI":"10.1093\/hmg\/11.25.3231","article-title":"SLUG (SNAI2) deletions in patients with Waardenburg disease","volume":"11","author":"M S\u00e1nchez-Mart\u00edn","year":"2002","journal-title":"Hum Mol Genet"},{"issue":"3","key":"ref63","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1002\/ajmg.10172","article-title":"ABCD syndrome is caused by a homozygous mutation in the EDNRB gene","volume":"108","author":"JB Verheij","year":"2002","journal-title":"Am J Med Genet"},{"issue":"4","key":"ref64","doi-asserted-by":"crossref","first-page":"442","DOI":"10.1038\/ng0496-442","article-title":"Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)","volume":"12","author":"P Edery","year":"1996","journal-title":"Nat Genet"},{"issue":"4","key":"ref65","doi-asserted-by":"crossref","first-page":"445","DOI":"10.1038\/ng0496-445","article-title":"A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)","volume":"12","author":"RM Hofstra","year":"1996","journal-title":"Nat Genet"},{"issue":"1","key":"ref66","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1111\/pcmr.12167","article-title":"Increasing the complexity: new genes and new types of albinism","volume":"27","author":"L Montoliu","year":"2014","journal-title":"Pigment Cell Melanoma Res"},{"issue":"2","key":"ref67","doi-asserted-by":"crossref","first-page":"176","DOI":"10.1111\/pcmr.12051","article-title":"Hermansky-Pudlak syndrome: pigmentary and non-pigmentary defects and their pathogenesis","volume":"26","author":"AH Wei","year":"2013","journal-title":"Pigment Cell Melanoma Res"},{"issue":"9","key":"ref68","doi-asserted-by":"crossref","first-page":"741","DOI":"10.1111\/j.1600-0625.2009.00896.x","article-title":"A review of genetic disorders of hypopigmentation: lessons learned from the biology of melanocytes","volume":"18","author":"C Dessinioti","year":"2009","journal-title":"Exp Dermatol"},{"issue":"10","key":"ref69","doi-asserted-by":"crossref","first-page":"3850","DOI":"10.1096\/fj.10-158485","article-title":"Melanocortin 1 receptor genotype: an important determinant of the damage response of melanocytes to ultraviolet radiation","volume":"24","author":"AL Kadekaro","year":"2010","journal-title":"FASEB J"},{"key":"ref70","doi-asserted-by":"crossref","first-page":"E18","DOI":"10.1111\/j.1749-6632.2010.05943.x","article-title":"Genetics and epigenetics of the X chromosome","volume":"1214","author":"C Morey","year":"2010","journal-title":"Ann N Y Acad Sci"}],"container-title":["PLOS ONE"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/dx.plos.org\/10.1371\/journal.pone.0171449","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,7,23]],"date-time":"2022-07-23T18:39:42Z","timestamp":1658601582000},"score":1,"resource":{"primary":{"URL":"https:\/\/dx.plos.org\/10.1371\/journal.pone.0171449"}},"subtitle":[],"editor":[{"given":"Andrzej T","family":"Slominski","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"editor"}]}],"short-title":[],"issued":{"date-parts":[[2017,2,7]]},"references-count":70,"journal-issue":{"issue":"2","published-online":{"date-parts":[[2017,2,7]]}},"URL":"https:\/\/doi.org\/10.1371\/journal.pone.0171449","relation":{},"ISSN":["1932-6203"],"issn-type":[{"value":"1932-6203","type":"electronic"}],"subject":[],"published":{"date-parts":[[2017,2,7]]}}}