Various Genital and Reproductive Phenotypes in 46,XX/46,XY Chimeras
Agathe Hercent(Inserm), Jean‐Pierre Siffroi(Sorbonne Université), Isabelle Goubin-Versini(Centre Hospitalier René-Dubos), Hélène Morel(Inserm), Régine Battin-Bertho(Lyon 1 Université), Edouard Amar(Clinique Victor Hugo), Frédérique Dijoud, Sandra Chantot‐Bastaraud(Fondation de Rothschild), Xavier Ferraretto(Lyon 1 Université), Stéphanie Belloc(Hôpital Lariboisière), Anne Claude Tabet(Hôpital Robert-Debré), Alexander Valent(Institut Gustave Roussy), Caroline Storey(Université Paris Cité), Jean‐François Hermieu(Assistance Publique – Hôpitaux de Paris), Matthieu Peycelon(Inserm)
Cited by 9
Related Papers
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
|PLoS Genetics|2014|672
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
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