Cargando…
CORRIGENDUM FOR “The Natural History of a Man With Ovotesticular 46,XX DSD Due to a Novel 3-Mb 15q26.2 Deletion Containing NR2F2 Gene”
Formato: | Online Artículo Texto |
---|---|
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063982/ https://www.ncbi.nlm.nih.gov/pubmed/32175518 http://dx.doi.org/10.1210/jendso/bvaa022 |
Ejemplares similares
-
The Natural History of a Man With Ovotesticular 46,XX DSD Caused by a Novel 3-Mb 15q26.2 Deletion Containing NR2F2 Gene
por: Carvalheira, Gianna, et al.
Publicado: (2019) -
THU189 Complex Treatment Of Recurrent Gynecomastia In An Affirmed Male With 46XX Ovotesticular Difference Of Sexual Differentiation (DSD).
por: Jumani, Sanjay, et al.
Publicado: (2023) -
A Novel WT1 Mutation Identified in a 46,XX Testicular/Ovotesticular DSD Patient Results in the Retention of Intron 9
por: Sirokha, Dmytro, et al.
Publicado: (2021) -
Leydig Cell Tumor in a Patient with 46,XX Disorder of Sex Development (DSD), Ovotesticular: A Case Report and a Review of the Literature
por: Gretser, Steffen, et al.
Publicado: (2021) -
NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development
por: Baetens, Dorien, et al.
Publicado: (2017)