Kimia Najafi
6PUBLICATIONS
15CO-AUTHORS

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Publications (6)
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|Nov 02, 2022
5p13 microduplication in a malformed fetus and his unaffected father.Ariana Kariminejad, Siavash Ghaderi-Sohi, Soheila Gholami
|Mar 27, 2021
Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities.Kimia Najafi, Zohreh Mehrjoo, Fariba Ardalani
|Jun 19, 2019
Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases.Kimia Najafi, Soheila Gholami, Azadeh Moshtagh
|Jun 12, 2019
Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient.Maryam Taghdiri, Atie Kashef, Golemaryam Abbassi
|Jan 31, 2017
Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis.Kimia Najafi, Roxana Kariminejad, Kaveh Hosseini
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Frequent Collaborators
1 joint publications
Atie Kashef
1 joint publications
Masood Bazrgar
1 joint publications
Roxana Kariminejad
1 joint publications
Ariana Kariminejad
1 joint publications
Soheil Rahmati
1 joint publications
Mohammadreza Alinejadfard
1 joint publications
Yasaman Zarinfar
1 joint publications
Amir Moradi
1 joint publications
Amir Ghabousian
1 joint publications
Ali Moradi