A De Novo Xp11.23 Duplication in a Girl with a Severe Phenotype: Expanding the Clinical Spectrum

بواسطة Arican, Pinar, Cavusoglu, Dilek, Gencpinar, Pinar, Ozyilmaz, Berk, Ozdemir, Taha Resid, Dundar, Nihal Olgac
الحاوية / القاعدة J Pediatr Genet (2018)

Various Neurological Symptoms with Vitamin B12 Deficiency and Posttreatment Evaluation

بواسطة Arıcan, Pinar, Bozkurt, Oznur, Cavusoglu, Dilek, Gencpınar, Pinar, Haspolat, Senay, Duman, Ozgur, Olgac Dundar, Nihal
الحاوية / القاعدة J Pediatr Neurosci (2020)

Chromosomal Microarray Analysis in Children with Unexplained Developmental Delay/Intellectual Disability

بواسطة Arican, Pinar, Olgac Dundar, Nihal, Ozyilmaz, Berk, Cavusoglu, Dilek, Gencpinar, Pinar, Erdogan, Kadri Murat, Saka Guvenc, Merve
الحاوية / القاعدة J Pediatr Genet (2019)