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Publikováno v:
American journal of medical genetics. 99(1)
Marfan syndrome (MFS) is an autosomal dominant disorder of connective tissue with marked interfamilial and intrafamilial variation in phenotype. The primary defect in affected patients resides in the gene for fibrillin-1 (FBN1) on 15q21. Linkage anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::364ef83714c57b55fd2c201b5cb43a26
https://pubmed.ncbi.nlm.nih.gov/11170092
https://pubmed.ncbi.nlm.nih.gov/11170092
