scholarly journals A novel WT1 gene mutation in a chinese girl with denys‐drash syndrome

2021 ◽  
Author(s):  
Faliang Wang ◽  
Jiabin Cai ◽  
Jinhu Wang ◽  
Min He ◽  
Junqing Mao ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Wt1 Gene ◽  
Chinese Girl ◽  
Drash Syndrome

Association of Partial Gonadal Dysgenesis, Nephropathy and WT1 Gene Mutation Without Wilms' Tumor: Incomplete Denys-Drash Syndrome

2001 ◽  
Vol 14 (5) ◽  
Author(s):  
E. Çetinkaya ◽  
G. Öcal ◽  
Μ. Berberoǧlu ◽  
P. Adiyaman ◽  
M. Ekim ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Gonadal Dysgenesis ◽  
Wilms Tumor ◽  
Wt1 Gene ◽  
Partial Gonadal Dysgenesis ◽  
Drash Syndrome

The Novel WT1 Gene Mutation p.H377N Associated to Denys-Drash Syndrome

2010 ◽  
Vol 32 (6) ◽  
pp. 486-488 ◽  
Author(s):  
Mara Sanches Guaragna ◽  
Fernanda Caroline Soardi ◽  
Juliana Godoy Assumpção ◽  
Lílian de Jesus Girotto Zambaldi ◽  
Izilda Aparecida Cardinalli ◽  
...  
Keyword(s):  
Gene Mutation ◽  
The Novel ◽  
Wt1 Gene ◽  
Drash Syndrome

scholarly journals Topotecan distribution in an anephric infant with therapy resistant bilateral Wilms tumor with a novel germline WT1 gene mutation

2008 ◽  
Vol 62 (6) ◽  
pp. 1039-1044 ◽  
Author(s):  
Rieneke T. Lugtenberg ◽  
Karlien Cransberg ◽  
Walter J. Loos ◽  
Anja Wagner ◽  
Marielle Alders ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Wilms Tumor ◽  
Wt1 Gene ◽  
Bilateral Wilms Tumor

scholarly journals A Novel WT1 Gene Mutation Associated with Wilms' Tumor and Congenital Male Genitourinary Malformation

2001 ◽  
Vol 50 (3) ◽  
pp. 337-344 ◽  
Author(s):  
Jun Sakamoto ◽  
Ayako Takata ◽  
Ryuji Fukuzawa ◽  
Haruhito Kikuchi ◽  
Masahiko Sugiyama ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Wilms Tumor ◽  
Wt1 Gene

scholarly journals Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq)

2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Yuhong Ye ◽  
Jingjing Wang ◽  
Xiaofang Quan ◽  
Ke Xu ◽  
Haidong Fu ◽  
...  
Keyword(s):  
Case Report ◽  
Turner Syndrome ◽  
Gene Mutation ◽  
Dent Disease ◽  
Clcn5 Gene ◽  
Chinese Girl

A newly identified exonic mutation of the WT1 gene in a patient with Denys-Drash syndrome

1996 ◽  
Vol 38 (3) ◽  
pp. 265-266 ◽  
Author(s):  
MASAHIKO TSUDA ◽  
TAKESHI SAKIYAMA ◽  
MISAO OWADA ◽  
YASUSHI CHIBA
Keyword(s):  
Wt1 Gene ◽  
Drash Syndrome

Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twins

2001 ◽  
Vol 16 (3) ◽  
pp. 227-231 ◽  
Author(s):  
Vikas R. Dharnidharka ◽  
E. Cristy Ruteshouser ◽  
Seymour Rosen ◽  
Harry Kozakewich ◽  
H. William Harris Jr. ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Wilms Tumor ◽  
Wilms Tumor 1 ◽  
Drash Syndrome

A novel insertional mutation at the third zinc finger coding region of the WT1 gene in Denys— Drash syndrome

1993 ◽  
Vol 2 (2) ◽  
pp. 203-204 ◽  
Author(s):  
O. Ogawa ◽  
M.R. Eccles ◽  
K. Yun ◽  
R.F. Mueller ◽  
M.D.D. Holdaway ◽  
...  
Keyword(s):  
Zinc Finger ◽  
Wt1 Gene ◽  
Coding Region ◽  
Insertional Mutation ◽  
The Third ◽  
Drash Syndrome

A NOVEL MISSENSE MUTATION OF THE WT1 GENE CAUSING DENYS-DRASH SYNDROME WITH EXCEPTIONALLY MILD RENAL MANIFESTATIONS

2000 ◽  
Vol 163 (6) ◽  
pp. 1857-1858 ◽  
Author(s):  
SHOICHIRO OHTA ◽  
TETSUO OZAWA ◽  
KIYOSHI IZUMINO ◽  
NOBUO SAKURAGAWA ◽  
HIDEKI FUSE
Keyword(s):  
Missense Mutation ◽  
Wt1 Gene ◽  
Drash Syndrome
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