Publisher: Karger
E-ISSN: 1423-0062|49|3|176-177
ISSN: 0001-5652
Source: Human Heredity, Vol.49, Iss.3, 1999-05, pp. : 176-177
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Related content
Novel FBN1 mutation in a family with inherited Marfan Syndrome: p.Cys2672Arg
CONGENITAL ANOMALIES, Vol. 58, Iss. 1, 2018-01 ,pp. :
By Mátyás Gábor Alonso Sira Patrignani Andrea Marti Myriam Arnold Eliane Magyar István Henggeler Caroline Carrel Thierry Steinmann Beat Berger Wolfgang
Human Genetics, Vol. 122, Iss. 1, 2007-08 ,pp. :
Human Heredity, Vol. 50, Iss. 3, 2000-02 ,pp. :
A Novel Fibrillin 1 Gene Mutation Leading to Marfan Syndrome with Minimal Cardiac Features
Molecular Syndromology, Vol. 5, Iss. 5, 2014-02 ,pp. :