Literature DB >> 12161615

A necropsy case of Denys-Drash syndrome with a WT1 mutation in exon 7.

R Fukuzawa1, J Sakamoto, R W Heathcott, J-I Hata.   

Abstract

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Year:  2002        PMID： 12161615      PMCID： PMC1735197          DOI： 10.1136/jmg.39.8.e48

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  4 in total

1.  Atypical clinical presentation of a WT1-related syndrome associated with a novel exon 6 gene mutation.

Authors:  Pietro Dattolo; Marco Allinovi; Paraskevas Iatropoulos; Stefano Michelassi
Journal:  BMJ Case Rep       Date:  2013-05-27

2.  Evolutive study of children with diffuse mesangial sclerosis.

Authors:  Ana Pilar Nso Roca; Antonia Peña Carrión; Marta Benito Gutiérrez; Carmen García Meseguer; Araceli García Pose; Mercedes Navarro
Journal:  Pediatr Nephrol       Date:  2008-12-10       Impact factor: 3.714

3.  New mutation in WT1 gene in a boy with an incomplete form of Denys-Drash syndrome: A CARE-compliant case report.

Authors:  Nail R Akramov; Rafael F Shavaliev; Ilsiya V Osipova
Journal:  Medicine (Baltimore)       Date:  2021-05-14       Impact factor: 1.889

4.  Exonic WT1 pathogenic variants in 46,XY DSD associated with gonadoblastoma.

Authors:  Sneha Arya; Sandeep Kumar; Anurag R Lila; Vijaya Sarathi; Saba Samad Memon; Rohit Barnabas; Hemangini Thakkar; Virendra A Patil; Nalini S Shah; Tushar R Bandgar
Journal:  Endocr Connect       Date:  2021-11-25       Impact factor: 3.335
  4 in total

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