Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program

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Bibliographic Details
Published inAmerican journal of medical genetics. Part A Vol. 185; no. 5; pp. 1498 - 1503
Main Authors Jarmolowicz, Anna I, Baker, Emma K, Bartlett, Essra, Francis, David, Ling, Ling, Gamage, Dinusha, Delatycki, Martin B, Godler, David E
Format Report
LanguageEnglish
Published 01.05.2021
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ISSN:1552-4833
DOI:10.1002/ajmg.a.62106