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ArticlesPeer ReviewedFull Text
A Novel Missense Mutation in the TGF-β-binding Protein-Like Domain 3 of FBN1 Causes Weill–Marchesani Syndrome with Intellectual Disability
Author / Creator:Hassani, Mahdieh ; Taghizadeh, Sara ; Farahzad Broujeni, Anahita ; Habibi, Mahvash ; Banitalebi, Setareh ; Kasiri, Mahbubeh ; Sadeghi, Alireza ; Nozari, Ahoura
Publisher:India: Wolters Kluwer - Medknow
Journal title:Advanced biomedical research, 2023-01, Vol.12 (1), p.114-114
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Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies
Author / Creator:Mohammadzadeh, Akbar ; Akbaroghli, Susan ; Aghaei-Moghadam, Ehsan ; Mahdieh, Nejat ; Badv, Reza Shervin ; Jamali, Payman ; Kariminejad, Roxana ; Chavoshzadeh, Zahra ; Ghasemi Firouzabadi, Saghar ; Mansour Ghanaie, Roxana ; Nozari, Ahoura ; Banihashemi, Sussan ; Hadipour, Fatemeh ; Hadipour, Zahra ; Kariminejad, Ariana ; Najmabadi, Hossein ; Shafeghati, Yousef ; Behjati, Farkhondeh
Publisher:Iran: Royan Institute of Iran
Journal title:Cell journal (Yakhteh), 2019-10, Vol.21 (3), p.337-349
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A Pathogenic Homozygous Mutation In The Pleckstrin Homology Domain Of RASA1 Is Responsible For Familial Tricuspid Atresia In An Iranian Consanguineous Family A Pathogenic Homozygous Mutation In The Pl...
Author / Creator:Ahoura Nozari ; Ehsan Aghaei-Moghadam ; Aliakbar Zeinaloo ; Afagh Alavi ; Saghar Ghasemi Firouzabad ; Shohre Minaee ; Marzeieh Eskandari Hesari ; Farkhondeh Behjati
Publisher:Royan Institute (ACECR), Tehran
Journal title:Cell journal (Yakhteh), 2018-12, Vol.21 (1), p.70-77
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A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family
Author / Creator:Nozari, Ahoura ; Aghaei-Moghadam, Ehsan ; Zeinaloo, Aliakbar ; Alavi, Afagh ; Ghasemi Firouzabdi, Saghar ; Minaee, Shohre ; Eskandari Hesari, Marzieh ; Behjati, Farkhondeh
Publisher:Iran: Royan Institute of Iran
Journal title:Cell journal (Yakhteh), 2019-04, Vol.21 (1), p.70-77
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A Novel Missense Mutation in the TGF-β-binding Protein-Like Domain 3 of FBN1 Causes Weill–Marchesani Syndrome with Intellectual Disability

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Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies

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A Pathogenic Homozygous Mutation In The Pleckstrin Homology Domain Of RASA1 Is Responsible For Familial Tricuspid Atresia In An Iranian Consanguineous Family A Pathogenic Homozygous Mutation In The Pl...

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A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family

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