Genotype and Phenotype Analysis of 171 Patients Referred for Molecular Study of the Fibrillin-1 Gene FBN1 Because of Suspected Marfan Syndrome
Year: 2001
Type: article
Study design: Observational Study
Source: Archives of Internal Medicine
Authors: B. Loeys, L Nuytinck, I Delvaux, S De Bie, A De Paepe
Institution: Ghent University Hospital
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2103147348