Literature DB >> 14228682

[THE ALDRICH SYNDROME; A CLINICAL AND GENETIC STUDY OF SEVERAL DUTCH FAMILIES].

J VAN DEN BOSCH, J DRUKKER.   

Abstract

Entities:  

Keywords:  ALDRICH SYNDROME; GENETICS, HUMAN

Mesh：

Year:  1964        PMID： 14228682

Source DB:  PubMed          Journal:  Maandschr Kindergeneeskd        ISSN： 0024-869X


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  2 in total

1.  Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WAS.

Authors:  L D Notarangelo; O Parolini; F Porta; F Locatelli; A Lanfranchi; M Marconi; L Nespoli; A Albertini; I W Craig; A G Ugazio
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

2.  N-WASP is a putative tumour suppressor in breast cancer cells, in vitro and in vivo, and is associated with clinical outcome in patients with breast cancer.

Authors:  Tracey A Martin; Gordon Pereira; Gareth Watkins; Robert E Mansel; Wen G Jiang
Journal:  Clin Exp Metastasis       Date:  2007-11-06       Impact factor: 5.150
  2 in total

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