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عناصر مشابهة

• Non-Syndromic Autosomal Recessive Deafness in Gaza Strip: A Study on Selected Connexin 26 Gene Mutations
  بواسطة: Essammak, Badria F. منشور: (2014)
• Genomic Studies of Autosomal Recessive Epilepsies in Three Omani Consanguineous Families
  بواسطة: Basak, Saroma منشور: (2016)
• Mutation Analysis of KIF13B as A Candidate Gene for Autosomal Recessive Hereditary Spastic Paraplegia
  بواسطة: Al-Barwani, Hamida Sarhan منشور: (2006)
• Bioinformatic and Functional Analyses of Single Nucleotide Polymorphism in Gene Found by Genome-Wide Pharmacogenetic Study to be Associated with the Outcome of Nortriptyline in the GENDEP Project
  بواسطة: Obaid, Rami منشور: (2009)
• Screening for mutations in B-cardiac myosin heavy chain gene among Jordanian patients with familial hypertrophic cardiomyopathy.
  بواسطة: Habbab, Wesal Marwan منشور: (2007)