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Anophthalmia-Waardenburg syndrome: A report of three cases

dc.contributor.authorCenani, A
dc.contributor.authorKartal, A
dc.contributor.authorSuyugul, N
dc.contributor.authorHacihanefioglu, S
dc.contributor.authorSeven, M
dc.contributor.authorSuyugul, Z
dc.date.accessioned2021-03-06T20:35:55Z
dc.date.available2021-03-06T20:35:55Z
dc.date.issued1996
dc.identifier.citationSuyugul Z., Seven M., Hacihanefioglu S., Kartal A., Suyugul N., Cenani A., "Anophthalmia-Waardenburg syndrome: A report of three cases", AMERICAN JOURNAL OF MEDICAL GENETICS, cilt.62, ss.391-397, 1996
dc.identifier.issn0148-7299
dc.identifier.otherav_fae8ac14-f0df-45eb-839f-b7fb1ce83b38
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/164265
dc.description.abstractWe report on 2 Turkish families with children who had bilateral anophthalmia, upper and lower limb abnormalities, mental retardation and consanguineous parents, We have evaluated the 2 cases in the first family and the only case in the second as anophthalmia-Waardenburg syndrome, This is an extremely rare autosomal recessive syndrome. (C) 1996 Wiley-Liss, Inc.
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.titleAnophthalmia-Waardenburg syndrome: A report of three cases
dc.typeMakale
dc.relation.journalAMERICAN JOURNAL OF MEDICAL GENETICS
dc.contributor.department, ,
dc.identifier.volume62
dc.identifier.issue4
dc.identifier.startpage391
dc.identifier.endpage397
dc.contributor.firstauthorID117404


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