Publications by authors named "Azadeh Hoseini"

Claim this Profile
W
Whole exome sequencing identifies novel pathogenic variants in TGM1 and ALOX12B in patients with hereditary ichthyosis.
Mitra Chegini, Maryam Eslami, Mahsa Motavaf, Omid Memarsadeghi, Azadeh Hoseini, Fatemeh Hoseininasab

Arch Dermatol Res· December 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of a novel de novo variant in in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosis.
Maryam Rafati, Faezeh Mohamadhashem, Koosha Jalilian, Fatemeh Hoseininasab, Laya Fakhri, Azadeh Hoseini

Ophthalmic Genet· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE-diagnosis study (IMPRESsion).
Saeed R Ghaffari, Maryam Rafati, Mahdi Shadnoush, Shokooh Pourbabaee, Mohammad Aghighi, Azadeh Hoseini, Fatemeh Hoseininasab

Hum Mutat· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Detection of Aneuploidies in Products of Conception and Neonatal Deaths in Iranian Patients Using the Multiplex Ligation-Dependent Probe Amplification (MLPA).
Sara Khorami Sarvestani, Maryam Rafati, Haleh Soltanghoraee, Azadeh Hoseini, Azadeh Soltani

Avicenna J Med Biotechnol· January 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prenatal Diagnosis of Tyrosinemia Type 1 Using Next Generation Sequencing.
Maryam Rafati, Faezeh Mohamadhashem, Azadeh Hoseini, Somayeh Darzi Ramandi, Saeed Reza Ghaffari

Fetal Pediatr Pathol· March 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel ACVR1 mutation detected by whole exome sequencing in a family with an unusual skeletal dysplasia.
Maryam Rafati, Faezeh Mohamadhashem, Azadeh Hoseini, Fatemeh Hoseininasab, Saeed Reza Ghaffari

Eur J Med Genet· June 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Heterozygosity assessment of five STR loci located at 5q13 region for preimplantation genetic diagnosis of spinal muscular atrophy.
Asghar Korzebor, Pupak Derakhshandeh-Peykar, Mohsen Meshkani, Azadeh Hoseini, Maryam Rafati, Marzieh Purhoseini

Mol Biol Rep· January 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
"
"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements.
Maryam Rafati, Mohammad R Ghadirzadeh, Yaser Heshmati, Homeira Adibi, Zarrintaj Keihanidoust, Azadeh Hoseini, Marzieh Purhoseini

Mol Cytogenet· January 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
"
"Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes.
Maryam Rafati, Elaheh Seyyedaboutorabi, Mohammad R Ghadirzadeh, Yaser Heshmati, Homeira Adibi, Azadeh Hoseini, Marzieh Purhoseini

Mol Cytogenet· January 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis