GATA4 mutations are uncommon in patients with 46,XY disorders of sex development without heart anomaly
Main Authors: | Maki Igarashi, Kentaro Mizuno, Masafumi Kon, Satoshi Narumi, Yoshiyuki Kojima, Yutaro Hayashi, Tsutomu Ogata, Maki Fukami |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2018-01-01
|
Series: | Asian Journal of Andrology |
Online Access: | http://www.ajandrology.com/article.asp?issn=1008-682X;year=2018;volume=20;issue=6;spage=629;epage=631;aulast=Igarashi |
Similar Items
-
Cryptic genomic rearrangements in three patients with 46,XY disorders of sex development.
by: Maki Igarashi, et al.
Published: (2013-01-01) -
MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency.
by: Hirohito Shima, et al.
Published: (2018-01-01) -
Screening of MAMLD1 mutations in 70 children with 46,XY DSD: identification and functional analysis of two new mutations.
by: Nicolas Kalfa, et al.
Published: (2012-01-01) -
GATA-4 Variants in Two Unrelated Cases with 46, XY Disorder of Sex Development and Review of the Literature
by: Nurullah Çelik, et al.
Published: (2022-12-01) -
A prenatal case misunderstood as specimen confusion: 46,XY/46,XY chimerism
by: Lin Chen, et al.
Published: (2024-02-01)