P. Jamali

Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome

H. Najmabadi, H. Ghaedi, H. Darvish, 2016, Molecular Neurobiology.

Iranome: A catalog of genomic variations in the Iranian population

R. Malekzadeh, H. Poustchi, B. Timmermann, 2019, Human mutation.

Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications

H. Darvish, M. Raeisoon, F. Behjati, 2016, International journal of molecular and cellular medicine.

Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization

H. Najmabadi, F. Behjati, R. Vameghi, 2013, Indian journal of human genetics.

A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran

K. Kahrizi, H. Najmabadi, C. Nishimura, 2012, American journal of medical genetics. Part A.

A clinical and molecular genetic study of 112 Iranian families with primary microcephaly

H. Ropers, A. Tzschach, K. Kahrizi, 2010, Journal of Medical Genetics.

Identification of Chromosome Abnormalities in Subtelomeric Regions Using Multiplex Ligation Dependent Probe Amplification (MLPA) Technique in 100 Iranian Patients With Idiopathic Mental Retardation

K. Kahrizi, H. Najmabadi, F. Sajedi, 2013, Iranian Red Crescent medical journal.