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Cowden disease. Report a family and review.
Author(s): Longy M, Lacombe D
Source: ANNALES DE GENETIQUE    Volume: 39    Issue: 1    Pages: 35-42    Published: 1996  
Times Cited: 68     References: 37     
Abstract: A description of different members of the same family affected by Cowden disease gives us the opportunity of a detailled review of the literature concerning the phenotypic and genotypic characteristics of this disease. Muco-cutaneous, mammary, thyroid, intestinal, urogenital, bone and neuro-sensorial involvement are detailled as well as pattern of inheritance and the inter and intra familial variability of expressivity. The different attempts to identify the implicated gene(s) are presented but they have failed at the present time.
Document Type: Review
Language: English
Reprint Address: Longy, M (reprint author), INST BERGONIE, 180 RUE ST GENES, F-33076 BORDEAUX, FRANCE
Addresses:
1. HOP PELLEGRIN, SERV GENET MED, F-33076 BORDEAUX, FRANCE
Publisher: EXPANSION SCI FRANCAISE, 31 BLVD LATOUR MAUBOURG, 75007 PARIS, FRANCE
Subject Category: Genetics & Heredity
IDS Number: UJ536
ISSN: 0003-3995
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