Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient von Taghdiri, Maryam, Kashef, Atie, Abbassi, Golemaryam, Moshtagh, Azadeh, Sadatian, Neda, Fardaei, Majid, Najafi, Kimia, Kariminejad, Roxana

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

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Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis von Kariminejad, Mohamad Hassan, Kariminejad, Ariana, Sadatian, Neda, Abbassi, Gole Maryam, Moshtagh, Azadeh, Hosseini, Kaveh, Kariminejad, Roxana, Najafi, Kimia, Bazrgar, Masood

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Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient von Taghdiri, Maryam, Kashef, Atie, Abbassi, Golemaryam, Moshtagh, Azadeh, Sadatian, Neda, Fardaei, Majid, Najafi, Kimia, Kariminejad, Roxana

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Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis von Najafi, Kimia, Kariminejad, Roxana, Hosseini, Kaveh, Moshtagh, Azadeh, Abbassi, Gole Maryam, Sadatian, Neda, Bazrgar, Masood, Kariminejad, Ariana, Kariminejad, Mohamad Hassan

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