Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleFragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.AuthorsJarmolowicz, Anna I.; Baker, Emma K.; Bartlett, Essra; Francis, David; Ling, Ling; Gamage, Dinusha; Delatycki, Martin B.; Godler, David E.PublicationAmerican Journal of Medical Genetics. Part A, 2021, Vol 185, Issue 5, p1498ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.62106