سامانه مدیریت امور پژوهشی دانشگاه مازندران | کوونی راونزایج ارت

	عنوان	مجله
1	A novel homozygous insertion and review of published mutations in the NNT gene causing familial glucocorticoid deficiency (FGD)	European Journal of Medical Genetics
2	Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly	BMC Medical Genomics