Informative STR Markers for Marfan Syndrome in Birjand, Iran

OBJECTIVE(S): Marfan syndrome (MFS) is a severe connective tissue disorder withan autosomal dominant inheritance pattern. Early diagnosis is critical in MFS. Because of the large size of fibrillin-1 gene (FBN1), the uniqueness of mutations, and the absence of genotype-to-phenotype correlations linka...

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Detalles Bibliográficos
Autores principales: Dadkhah, Ezzat, Ziaee, Masood, Davari, Mohammad Hossein, Kazemi, Toba, Abbaszadegan, Mohammad Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586928/
https://www.ncbi.nlm.nih.gov/pubmed/23493941

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586928/
https://www.ncbi.nlm.nih.gov/pubmed/23493941

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