Literature DB >> 23835859

Patients with different or identical genotypes of the WT1 gene present different phenotypes.

Yonghui Yang1, Feng Zhao, Jun Huang, Xiaojing Nie, Zihua Yu.   

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Year:  2013        PMID： 23835859     DOI： 10.1007/s00431-013-2086-4

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  8 in total

1.  Constitutional WT1 correlate with clinical features in children with progressive nephropathy.

Authors:  A Takata; H Kikuchi; R Fukuzawa; S Ito; M Honda; J Hata
Journal:  J Med Genet       Date:  2000-09       Impact factor: 6.318

2.  A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndrome.

Authors:  N Hakan; M Aydin; O Erdogan; Y H Cavusoglu; Z Aycan; F Ozaltin; A Zenciroglu; S Apaydin; R Gunes; G Sahin; G Cinar; N Okumus
Journal:  Genet Couns       Date:  2012

3.  Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations.

Authors:  Gil Chernin; Virginia Vega-Warner; Dominik S Schoeb; Saskia F Heeringa; Bugsu Ovunc; Pawaree Saisawat; Roxana Cleper; Fatih Ozaltin; Friedhelm Hildebrandt
Journal:  Clin J Am Soc Nephrol       Date:  2010-07-01       Impact factor: 8.237

4.  Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome.

Authors:  Filip Fencl; Michal Malina; Veronika Stará; Jakub Zieg; Dana Mixová; Tomáš Seeman; Květa Bláhová
Journal:  Eur J Pediatr       Date:  2011-05-26       Impact factor: 3.183

Review 5.  The Denys-Drash syndrome.

Authors:  R F Mueller
Journal:  J Med Genet       Date:  1994-06       Impact factor: 6.318

6.  A child with isolated nephrotic syndrome and WT1 mutation presenting as a 46, XY phenotypic male.

Authors:  Yonghui Yang; Dongning Feng; Jun Huang; Xiaojing Nie; Zihua Yu
Journal:  Eur J Pediatr       Date:  2012-07-05       Impact factor: 3.183

Review 7.  Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations.

Authors:  Geneviève Benoit; Eduardo Machuca; Corinne Antignac
Journal:  Pediatr Nephrol       Date:  2010-03-24       Impact factor: 3.714

8.  Discordant phenotypes in monozygotic twins with identical de novo WT1 mutation.

Authors:  Zihua Yu; Yonghui Yang; Dongning Feng
Journal:  Clin Kidney J       Date:  2012-04-02
  8 in total

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