Výsledky vyhledávání - "Faïza Fakhfekh"

A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1

Autor: Mounira Hmani-Aifa, Hammadi Ayadi, Faïza Fakhfekh, Khalil Turki, Peter Söderkvist, Riadh Messaoud, Moncef Khairallah, Salma Ben Salem, Ahmed Rebai, Walid Bouassida, Zeineb Benzina

Publikováno v: Human genetics. 126(4)

Posterior microphthalmia (PM) is a relatively rare autosomal recessive condition with normal anterior segment and small posterior segment resulting in high hyperopia and retinal folding. It is an uncommon subtype of microphthalmia that has been mostl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73656537bd66fd5879743b4628d176ba
https://pubmed.ncbi.nlm.nih.gov/19526372

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