Literature DB >> 8111391

A novel zinc finger mutation in a patient with Denys-Drash syndrome.

P N Baird1, J K Cowell.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8111391     DOI: 10.1093/hmg/2.12.2193

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


× No keyword cloud information.
  2 in total

1.  Software and database for the analysis of mutations in the human WT1 gene.

Authors:  C Jeanpierre; C Béroud; P Niaudet; C Junien
Journal:  Nucleic Acids Res       Date:  1998-01-01       Impact factor: 16.971

2.  Screening 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.

Authors:  Annes Siji; Varsha Chhotusing Pardeshi; Shilpa Ravindran; Ambily Vasudevan; Anil Vasudevan
Journal:  BMC Med Genet       Date:  2017-01-10       Impact factor: 2.103

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.