Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities

por Najafi, Kimia, Mehrjoo, Zohreh, Ardalani, Fariba, Ghaderi-Sohi, Siavash, Kariminejad, Ariana, Kariminejad, Roxana, Najmabadi, Hossein
Publicado 2021

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

por Taghdiri, Maryam, Kashef, Atie, Abbassi, Golemaryam, Moshtagh, Azadeh, Sadatian, Neda, Fardaei, Majid, Najafi, Kimia, Kariminejad, Roxana
Publicado 2019

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

por Najafi, Kimia, Kariminejad, Roxana, Hosseini, Kaveh, Moshtagh, Azadeh, Abbassi, Gole Maryam, Sadatian, Neda, Bazrgar, Masood, Kariminejad, Ariana, Kariminejad, Mohamad Hassan
Publicado 2017

Kaufman Oculo-cerebro-facial Syndrome in a child with small and absent terminal phalanges and absent nails

por Kariminejad, Ariana, Ajeawung, Norbert Fonya, Bozorgmehr, Bita, Dionne-Laporte, Alexandre, Molidperee, Sirinart, Najafi, Kimia, Gibbs, Richard A, Lee, Brendan H, Hennekam, Raoul C, Campeau, Philippe M
Publicado 2016

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

por Najafi, Kimia, Gholami, Soheila, Moshtagh, Azadeh, Bazrgar, Masood, Sadatian, Neda, Abbasi, Golemaryam, Rostami, Parvin, Khalili, Soheila, Babanejad, Mojgan, Nourmohammadi, Bahareh, Faramarzi Garous, Negin, Najmabadi, Hossein, Kariminejad, Roxana
Publicado 2019