Memnune Yüksel‐Apak

Mutations in different components of FGF signaling in LADD syndrome

Edyta Rohmann, Han G. Brunner, Hülya Kayserili et al. · Nature Genetics · 2006 · 207 citations

Developmental Biology, Mendelian Disorder, Human Growth +7

Mutations in Capillary Morphogenesis Gene-2 Result in the Allelic Disorders Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis

Oonagh Dowling, Analisa DiFeo, Maria Celeste M. Ramirez et al. · The American Journal of Human Genetics · 2003 · 195 citations · Full text

Developmental Anomaly, Fibrosis, Developmental Biology +5

A somatic origin of homologous Robertsonian translocations and isochromosomes

Wendy P. Robinson, Memnune Yüksel‐Apak, Giovanni Neri et al. · PubMed · 1994 · 129 citations · Full text

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