Implantation of cardiac defibrillator in an infant with hypertrophic cardiomyopathy and newly identified MYBP3 mutation

por Güvenç, Osman, Karaer, Kadri, Haydin, Sertaç, Güzeltaş, Alper, Ergül, Yakup
Publicado 2020

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy

por Demir, Korcan, Nalbantoğlu, Özlem, Karaer, Kadri, Korkmaz, Hüseyin Anıl, Yıldız, Melek, Tunç, Selma, Özkan, Behzat
Publicado 2015