Azadeh Moshtagh

Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases

H. Najmabadi, R. Kariminejad, M. Bazrgar, 2019, Molecular genetics & genomic medicine.

Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis

A. Kariminejad, K. Hosseini, R. Kariminejad, 2017, Case reports in genetics.

A Report on 167 Cases of Array-Based Comparative Genomic Hybridization: Comparison with Previous Techniques

A. Kariminejad, H. Najmabadi, F. Behjati, 2012 .

Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18

M. Okoniewski, A. Kariminejad, A. Schinzel, 2011, European Journal of Human Genetics.

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

M. Fardaei, R. Kariminejad, Maryam Taghdiri, 2019, Clinical case reports.

Evaluation of the Concordance of Sex Chromatin with Cytogenetic Findings: A Report of 9450 Cases Part One

M. Kariminejad, Soheila Gholami, Azadeh Moshtagh, 2013 .

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

M. Fardaei, R. Kariminejad, Maryam Taghdiri, 2019, Clinical case reports.