Preimplantation genetic diagnosis versus prenatal diagnosis—decision-making among pregnant FMR1 premutation carriers
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Developmental Biology,Obstetrics and Gynecology,Genetics,Reproductive Medicine,General Medicine
Link
http://link.springer.com/article/10.1007/s10815-018-1293-3/fulltext.html
Reference26 articles.
1. Wittenberger MD, Hagerman RJ, Sherman SL, McConkie-Rosell A, Welt CK, Rebar RW, et al. The FMR1 premutation and reproduction. Fertil Steril. 2007;87:456–65.
2. Nolin SL, Glicksman A, Ding X, et al. Fragile X analysis of 1112 natal samples from 1991 to 2010. Prenat Diagn. 2011;31(10):925 931–2011.
3. Tsafrir A, Altarescu G, Margalioth E, Brooks B, Renbaum P, Levy-Lahad E, et al. PGT-M for fragile X syndrome: ovarian function is the main determinant of success. Hum Reprod. 2010;25(10):2629–36.
4. Jin P, Warren ST. Understanding the molecular basis of fragile X syndrome. Hum Mol Genet. 2000;9:901–8.
5. Hoyos LR, Thakur M. Fragile X premutation in women: recognizing the health challenges beyond primary ovarian insufficiency. J Assist Reprod Genet. 2017;34(3):315–23.
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