View in EDS

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

Saved in:
Bibliographic Details
Title: Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.
Authors: Jarmolowicz, Anna I.1, anna.jarmolowicz@mcri.edu.au, Baker, Emma K.2,3,4, Bartlett, Essra1, Francis, David1, Ling, Ling2, Gamage, Dinusha2, Delatycki, Martin B.1,3, Godler, David E.2,3
Source: American Journal of Medical Genetics. Part A; May2021, Vol. 185 Issue 5, p1498-1503, 6p
Database: Applied Science & Technology Source
Be the first to leave a comment!
You must be logged in first