Portal de investigación
Towards an experimental proof of oligogenicity explaining a severe 46, XY DSD phenotype associated with heterozygote NR5A1/SF-1 variation
Fecha de publicación:
Autores de IIS La Fe
Participantes ajenos a IIS La Fe
- Naamneh-Elzenaty, Rawda
- Sauter, Kay-Sara
- Kouri, Chrysanthi
- de Lapiscina, Idoia Martinez
- Camats-Tarruella, Nuria
- Flueck, Christa E.
Grupos
Abstract
Abstract no disponible
Filiaciones
Filiaciones no disponibles
Cita
Naamneh,R,Sauter,K,Kouri,C,de Lapiscina,IM,Moreno,F,Camats,N,Flueck,CE. Towards an experimental proof of oligogenicity explaining a severe 46, XY DSD phenotype associated with heterozygote NR5A1/SF-1 variation. ALLSCHWILERSTRASSE 10, CH-4009 BASEL, SWITZERLAND:KARGER. 2024 p.p. 24-25.