Finding a single XY cell among XX cells in amniotic fluid by FISH: a possible consequence of a vanishing male twin?
Lieve Verstraete(Sorbonne Université), Nadia Berkane(Université Paris-Sud), Jean‐Pierre Siffroi(Sorbonne Université), Jean‐Marc Costa(Virbac (France)), Serge Uzan, Olivia Fiori(Sorbonne Université), Sandra Chantot‐Bastaraud(Fondation de Rothschild)
Cited by 6
Related Papers
In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene
|The American Journal of Human Genetics|2003|518
Human Male Infertility Associated with Mutations in NR5A1 Encoding Steroidogenic Factor 1
|The American Journal of Human Genetics|2010|247
KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes
|Nature Genetics|2011|244
From Pregnancy to Preeclampsia: A Key Role for Estrogens
|Endocrine Reviews|2017|225
Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia
|The American Journal of Human Genetics|2019|196