Výsledky vyhledávání - "Hussain Jafrid"

Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genes

Autor: Caroline B. Michielse, Yasmin Raashid, Hussain Jafrid, José A. J. M. van den Hurk, Han G. Brunner, Meena Bhat, George W. Padberg, Hans van Bokhoven, Angela F. Brady

Publikováno v: European Journal of Human Genetics, 14, 12, pp. 1306-12
European Journal of Human Genetics, 14, 1306-12

Contains fulltext : 50478.pdf (Publisher’s version ) (Closed access) Hereditary congenital facial palsy (HCFP) is an autosomal-dominant disorder consisting of paresis or paralysis of the VIIth (facial) cranial nerve. Genetic heterogeneity for this

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c50e30a894cc57d3ae3092a385ba9102
https://doi.org/10.1038/sj.ejhg.5201706

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání