Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities.
about
The Denys-Drash syndromeDown syndrome in association with features of the androgen insensitivity syndrome.Exclusion of WTAP and HOXA13 as candidate genes for isolated hypospadias.The genetics of male undermasculinization.Software and database for the analysis of mutations in the human WT1 geneAndrogen insensitivity syndrome: a survey of diagnostic procedures and management in the UKTranslational genetics for diagnosis of human disorders of sex developmentScreening of WT1 mutations in exon 8 and 9 in children with steroid resistant nephrotic syndrome from a single centre and establishment of a rapid screening assay using high-resolution melting analysis in a clinical setting.Perspectives in Pediatric Pathology, Chapter 5. Gonadal Dysgenesis.Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.Steroid-resistant nephrotic syndrome caused by novel WT1 mutation inherited from a mosaic parent.
P2860
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P2860
Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities.
description
1993 nî lūn-bûn
@nan
1993 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Mutational screening of the Wi ...... es with genital abnormalities.
@ast
Mutational screening of the Wi ...... es with genital abnormalities.
@en
type
label
Mutational screening of the Wi ...... es with genital abnormalities.
@ast
Mutational screening of the Wi ...... es with genital abnormalities.
@en
prefLabel
Mutational screening of the Wi ...... es with genital abnormalities.
@ast
Mutational screening of the Wi ...... es with genital abnormalities.
@en
P2093
P2860
P356
P1476
Mutational screening of the Wi ...... es with genital abnormalities.
@en
P2093
D M Williams
H R Davies
I A Hughes
P A Clarkson
R Chaudhary
P2860
P304
P356
10.1136/JMG.30.9.767
P407
P577
1993-09-01T00:00:00Z