Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program. - Jarmolowicz, Anna I.; Baker, Emma K.; Bartlett, Essra; Francis, David; Ling, Ling; Gamage, Dinusha; Delatycki, Martin B.; Godler, David E. (American Journal of Medical Genetics. Part A, 2021)