Molecular etiology, pathogenesis and diagnosis of the Marfan syndrome-Reference-Cited by-同舟云学术

Molecular etiology, pathogenesis and diagnosis of the Marfan syndrome

Published:1996-06 Issue:3 Volume:5 Page:159-166
ISSN:1058-9813
Container-title:Progress in Pediatric Cardiology
language:en
Short-container-title:Progress in Pediatric Cardiology

Author:

Dietz Harry C.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Pediatrics, Perinatology, and Child Health

Reference27 articles.

1. Un cas de de formation congenitale des quatre — membres plus prononcé aux extrémités charactériseée par l'allongement des os avec un certain degré d'amincissement;Marfan;Bull Mém Soc Méd Hôp Paris,1896

2. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene;Dietz;Nature,1991

3. Location on chromosome 15 of the gene defect causing Marfan syndrome;Kainulainen;N Engl J Med,1990

4. The Marfan syndrome locus: confirmation of assignment to chromosome 15 and identification of tightly linked markers at 15q15-q21.3;Dietz;Genomics,1991

5. Fibrillin, a new 350-kD glycoprotein, is a component of extracelluiar microfibrils;Sakai;J Cell Biol,1986

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