A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene

Por Keskin, Melikşah, Muratoğlu Şahin, Nursel, Kurnaz, Erdal, Bayramoğlu, Elvan, Savaş Erdeve, Şenay, Aycan, Zehra, Çetinkaya, Semra
Publicado no J Clin Res Pediatr Endocrinol (2017)

Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

Por Aycan, Zehra, Savaş-Erdeve, Şenay, Çetinkaya, Semra, Kurnaz, Erdal, Keskin, Melikşah, Muratoğlu Şahin, Nursel, Bayramoğlu, Elvan, Ceylaner, Gülay
Publicado no J Clin Res Pediatr Endocrinol (2018)

Antimüllerian Hormone Levels of Infants with Premature Thelarche

Por Muratoğlu Şahin, Nursel, Bayramoğlu, Elvan, Nursun Özcan, Hatice, Kurnaz, Erdal, Keskin, Melikşah, Savaş-Erdeve, Şenay, Çetinkaya, Semra, Aycan, Zehra
Publicado no J Clin Res Pediatr Endocrinol (2019)

A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make

Por Çetinkaya, Semra, Güran, Tülay, Kurnaz, Erdal, Keskin, Melikşah, Sağsak, Elif, Savaş Erdeve, Senay, Suntharalingham, Jenifer P., Buonocore, Federica, Achermann, John C., Aycan, Zehra
Publicado no J Clin Res Pediatr Endocrinol (2018)