Literature DB >> 23835858

Different clinical presentations of WT1 gene mutations.

Mustafa Aydin1, Nilay Hakan, Aysegul Zenciroglu, Ozlem Aydog, Nurullah Okumus.   

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Year:  2013        PMID： 23835858     DOI： 10.1007/s00431-013-2085-5

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


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  4 in total

Review 1.  WT1 and kidney progenitor cells.

Authors:  Jordan A Kreidberg
Journal:  Organogenesis       Date:  2010 Apr-Jun       Impact factor: 2.500

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

Review 3.  The Denys-Drash syndrome.

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

4.  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
  4 in total
  1 in total

1.  Spectrum of Clinical Manifestations in Children With WT1 Mutation: Case Series and Literature Review.

Authors:  Patricia Arroyo-Parejo Drayer; Wacharee Seeherunvong; Chryso P Katsoufis; Marissa J DeFreitas; Tossaporn Seeherunvong; Jayanthi Chandar; Carolyn L Abitbol
Journal:  Front Pediatr       Date:  2022-04-15       Impact factor: 3.418
  1 in total

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