Murat Derbent

Mutations in HPSE2 Cause Urofacial Syndrome

Sarah B. Daly, Jill Urquhart, Emma Hilton et al. · The American Journal of Human Genetics · 2010 · 108 citations · Full text

Urology, Genetic Disorder, Inherited Metabolic Disease +4

Mutations in <i>LONP1</i>, a mitochondrial matrix protease, cause CODAS syndrome

Esra Dikoglu, Ali Abdullah Alfaiz, Maria W. Górna et al. · American Journal of Medical Genetics Part A · 2015 · 81 citations

Chromosome 22q11.2 deletion and phenotypic features in 30 patients with conotruncal heart defects

Murat Derbent, Zerrin Yılmaz, Volkan Baltacı et al. · American Journal of Medical Genetics Part A · 2002 · 81 citations

Effect of Congenital Heart Disease on Renal Function in Childhood

Pınar Işık Ağras, Murat Derbent, Figen Özçay et al. · Nephron Physiology · 2004 · 58 citations

Propranolol for infantile hemangiomas: a preliminary report on efficacy and safety in very low birth weight infants.

Ayşe Erbay, Faik Sarıalioğlu, Barış Malbora et al. · PubMed · 2011 · 46 citations

Propranolol Treatment, Hypertension, Pediatric Hematology +11