Screening PAX9, MSX1 and WNT10A Mutations in 4 Iranian Families with Non-Syndromic Tooth Agenesis

por Safari, Shiva, Ebadifar, Asghar, Najmabadi, Hossien, Kamali, Koorosh, Abedini, Seyedeh Sedigheh
Publicado 2020

Detection of a rare AXIN2 variant in an Iranian family with hypodontia and oligodontia

por Safari, Shiva, Ebadifar, Asghar, Najmabadi, Hossien, Kamali, Koorosh, Abedini, Seyedeh Sedigheh, Mousavi, Mohammad
Publicado 2022

A Novel Deletion Mutation in ASPM Gene in an Iranian Family with Autosomal Recessive Primary Microcephaly

por AKBARIAZAR, Elinaz, EBRAHIMPOUR, Mohammad, AKBARI, Saeedeh, ARZHANGHI, Sanaz, ABEDINI, Seydeh Sedigheh, NAJMABADI, Hossein, KAHRIZI, Kimia
Publicado 2013

Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's Disease

por Mehrjoo, Zohreh, Najmabadi, Amin, Abedini, Seyedeh Sedigheh, Mohseni, Marzieh, Kamali, Koorosh, Najmabadi, Hossein, Khorram Khorshid, Hamid Reza
Publicado 2015

Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability

por Mehvari, Sepideh, Larti, Farzaneh, Hu, Hao, Fattahi, Zohreh, Beheshtian, Maryam, Abedini, Seyedeh Sedigheh, Arzhangi, Sanaz, Ropers, Hans‐Hilger, Kalscheuer, Vera M., Auld, Daniel, Kahrizi, Kimia, Riazalhosseini, Yasser, Najmabadi, Hossein
Publicado 2020

Chromosome abnormality rate among Iranian patients with idiopathic mental retardation from consanguineous marriages

por Behjati, Farkhondeh, Ghasemi Firouzabadi, Saghar, Kahrizi, Kimia, Kariminejad, Roxana, Bagherizadeh, Iman, Ansari, Javad, Fallah, Masoumeh, Mojtahedi, Forough, Darvish, Hossein, Bahrami Monajemi, Gholamreza, Abedini, S. Sedigheh, Jamali, Payman, Mojahedi, Faezeh, Zadeh-Vakili, Azita, Najmabadi, Hossein
Publicado 2011