Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Aneuploidy and FMR1[original query] |
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Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study. Genetics in medicine : official journal of the American College of Medical Genetics 2013 Apr 15 (4): 290-8. Inaba Yoshimi, Herlihy Amy S, Schwartz Charles E, Skinner Cindy, Bui Quang M, Cobb Joanna, Shi Elva Z, Francis David, Arvaj Alison, Amor David J, Pope Kate, Wotton Tiffany, Cohen Jonathan, Hewitt Jacqueline K, Hagerman Randi J, Metcalfe Sylvia A, Hopper John L, Loesch Danuta Z, Slater Howard R, Godler David |
Utilizing FMR1 gene mutations as predictors of treatment success in human in vitro fertilization. PloS one 2014 9 (7): e102274. Kushnir Vitaly A, Yu Yao, Barad David H, Weghofer Andrea, Himaya Eric, Lee Ho-Joon, Wu Yan-Guang, Shohat-Tal Aya, Lazzaroni-Tealdi Emanuela, Gleicher Norbe |
Maternal germline factors associated with aneuploid pregnancy loss: a systematic review. Human reproduction update 2021 . Blyth Ursula, Craciunas Laurentiu, Hudson Gavin, Choudhary Meenaks |
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