A Novel Mutation in the VPS13B Gene in a Cohen Syndrome Patient with Positive Antiphospholipid Antibodies

by Roghayeh Dehghan, Mahdiyeh Behnam, Alireza Moafi, Mansoor Salehi
Published 2021-01-01

Sirenomelia: two case reports

by Asiyeh Shojaee, Firooze Ronnasian, Mahdiyeh Behnam, Mansoor Salehi
Published 2021-04-01

A novel missense mutation in the GNE gene in an Iranian patient with hereditary inclusion body myopathy

by Mahdiyeh Behnam, Shin Jin-Hong, Dae-Seong Kim, Keivan Basiri, Yalda Nilipour, Maryam Sedghi
Published 2014-01-01

Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran

by Maryam Sedghi, Mahdiyeh Behnam, Esmat Fazel, Mansoor Salehi, Hamid Ganji, Rokhsareh Meamar, Majid Hosseinzadeh, Nayereh Nouri
Published 2014-01-01

Prevalence of 22q11.2 microdeletion syndrome in Iranian patients with cleft palate

by Narges Nouri, Mehrdad Memarzadeh, Mansoor Salehi, Nayereh Nouri, Rokhsareh Meamar, Mahdiyeh Behnam, Fatemeh Derakhshandeh, Tahereh Kashkoolinejad, Hossein Abdali
Published 2016-01-01

Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran

by Mohsen Reisi, Mahdiyeh Behnam, Seyed Javad Sayedi, Farzaneh Salimi, Pegah Kargar, Mansoor Salehi, Hossein Saneian, Iman Kashani, Roya Kelishadi
Published 2019-04-01