H. Ilgin-Ruhi

An Evaluation of the Phenotypic Features of Fanconi Anemia Together with DEB/MMC Positivity in 199 Turkish Patients

H. Karabulut, T. Tuncalı, A. Tükün, 2013 .

Molecular spectrum of PIK3CA gene mutations in patients with nonsmall-cell lung cancer in Turkey.

M. Dogan, A. Tukun, A. Demirkazık, 2015, Genetic testing and molecular biomarkers.

Axenfeld-Rieger syndrome associated with truncus arteriosus: a case report.

A. Yarangümeli, G. Kural, H. Ilgin-Ruhi, 2007, The Turkish journal of pediatrics.

The genotoxic effects of hepatitis B virus to host DNA.

A. Elhan, S. Kaçar, N. Şaşmaz, 2005, Mutagenesis.

Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development

H. Karabulut, Z. Aycan, Z. Şıklar, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

The role of genetic counseling on decisions of pregnant women aged 35 years or over regarding amniocentesis in Turkey.

A. Tükün, Nüket Yürür-Kutlay, H. Ilgin-Ruhi, 2005, European journal of medical genetics.