Gülay Ceylaner

Genetic abnormalities in Turkish women with premature ovarian failure

Gülay Ceylaner, Sündüz Özlem Altınkaya, Leyla Mollamahmutoğlu et al. · International Journal of Gynecology & Obstetrics · 2010 · 34 citations

A Novel Mutation in the Lysyl Hydroxylase 1 Gene Causes Decreased Lysyl Hydroxylase Activity in an Ehlers–Danlos VIA Patient

Linda C. Walker, Mayra A. Overstreet, Adnan H. Siddiqui et al. · Journal of Investigative Dermatology · 2005 · 22 citations · Full text

Lysyl Hydroxylase Activity, Mendelian Disorder, Genetic Disorder +10

Extremely skewed X‐chromosome inactivation patterns in women with recurrent spontaneous abortion

Sevgi Baǧışlar, Bora Cengiz, Feride Söylemez et al. · Australian and New Zealand Journal of Obstetrics and Gynaecology · 2006 · 22 citations

GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals

Elif Baysal, Yıldırım A. Bayazit, Serdar Ceylaner et al. · Journal of Genetics · 2008 · 19 citations

Healthy Individuals, Mendelian Disorder, Genetic Disorder +10

Postmortem evaluation of 220 prenatally diagnosed fetuses with neural tube defects: detection of associated anomalies in a Turkish population

Serdar Ceylaner, Gülay Ceylaner, İlker Günyeli et al. · Prenatal Diagnosis · 2006 · 17 citations