Asadollah Ghanbari

Frequencies of gap‐ and tight‐junction mutations in Turkish families with autosomal‐recessive non‐syndromic hearing loss

M Emiroglu, Abdullah Üzümcü, Asadollah Ghanbari et al. · Clinical Genetics · 2003 · 94 citations

Genetics, Molecular Genetics, Disease Gene Identification +19

Homozygous and heterozygous inheritance of <i>PAX3</i> mutations causes different types of Waardenburg syndrome

Bernd Wollnik, Turgut Tükel, Zehra Oya Uyguner et al. · American Journal of Medical Genetics Part A · 2003 · 79 citations

Genetics, Pathology, Heterozygous Inheritance +16

The novel R75Q mutation in the <i>GJB2</i> gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family

Turgut Tükel, Can Baykal, Hacer Eris et al. · Clinical Genetics · 2002 · 75 citations

Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases

Birsen Karaman, Hülya Kayserili, Asadollah Ghanbari et al. · Molecular Cytogenetics · 2018 · 29 citations · Full text

The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey

Birsen Karaman, Melike Aytan, Kader Yılmaz et al. · European Journal of Medical Genetics · 2005 · 12 citations

Karyotype Imaging, Cytogenetics, Spectral Karyotyping +4