AHI1 gene mutation in a consanguineous Iranian family affected by Joubert syndrome: A case report af Mostafa Neissi, Hadideh Mabudi, Javad Mohammadi‐Asl

Få fuldtekst

The worldwide molecular spectrum and distribution of thalassaemia: a systematic review af Mina Ebrahimi, Javad Mohammadi-Asl, Fakher Rahim

Få fuldtekst

Comparison of the effects of olsalazine and decitabine on the expression of CDH1 and uPA genes and cytotoxicity in MDA-MB-231 breast cancer cells af Misagh Mohammadi Asl, Javad Mohammadi Asl, Mojgan Naghitorabi

Få fuldtekst

Retinitis pigmentosa‐1 due to an RP1 mutation in a consanguineous Iranian family: Report of a novel mutation af Mostafa Neissi, Motahareh Sheikh‐Hosseini, Javad Mohammadi‐Asl

Få fuldtekst

A Novel Disease-Causing ASPA Gene Mutation (c.432+1 G>C) in an Iranian Patient with Canavan Disease: A Case Report af Mostafa Neissi, Motahareh Sheikh-Hosseini, Javad Mohammadi-Asl

Få fuldtekst

A Novel Deleterious MYO15A Gene Mutation Causes Nonsyndromic Hearing Loss af Mostafa Neissi, Adnan Al-Badran, Javad Mohammadi-Asl

Få fuldtekst

Exome sequencing identifies a novel GUCY2D mutation in an Iranian family with Leber congenital amaurosis-1: a case report af Mostafa Neissi, Adnan Issa Al-Badran, Javad Mohammadi-Asl

Få fuldtekst

An intelligent prenatal screening system for the prediction of Trisomy-21 af Amir Jamshidnezhad, Seyed Mohsen Hosseini, Javad Mohammadi-Asl, Mandana Mahmudi

Få fuldtekst

Evaluation of the effect of oral taurine supplementation on fasting levels of fibroblast growth factors, β-Klotho co-receptor, some biochemical indices and body composition in obes... af Fatemeh Haidari, Maryam Asadi, Javad mohammadi-asl, Kambiz Ahmadi-Angali

Få fuldtekst

Folate gene polymorphisms CBS 844ins68 and RFC1 A80G and risk of Down syndrome offspring in young Iranian women: A cross-sectional study af Neda Farajnezhad, Pegah Ghandil, Maryam Tahmasebi-Birgani, Javad Mohammadi-Asl

Få fuldtekst

Identification of a novel non-stop mutation in PDE6C gene in an Iranian family with Con-Rod Dystrophy af Shahram Nasiri, Farah Talebi, Javad Mohammadi Asl, Farideh Ghanbari Mardasi

Få fuldtekst

Identification of a Novel Frameshift Mutation in the TECTA Gene in an Iranian Family With Autosomal Nonsyndromic Hearing Loss af Javad Mohammadi-Asl, Nader Saki, Majid Karimi, Farideh Ghanbari Mardasi

Få fuldtekst

Do NGS‐based techniques represent a first‐line testing in suspected Duchenne muscular dystrophy? af Seyed Mohammad Hosseini, Nosratollah Alizadeh, Abolfazl Amini, Javad Mohammadi‐Asl

Få fuldtekst

Melatonin improves spermatogonial stem cells transplantation efficiency in azoospermic mice af Mohammadreza Gholami, Ghasem Saki, Masoud Hemadi, Ali Khodadadi, Javad Mohammadi-asl

Få fuldtekst

Up-regulation of SNHG5 Expression Level in Patients with Chronic Myeloid Leukemia Compared with Normal Individuals af Zahra Shahpouri-Arani, Mohamad Reza Hajari, Javad Mohammadi-Asl, Najmaldin Saki

Få fuldtekst

Exome sequencing identified a novel Col6α1 mutation in an Iranian patient with Ullrich congenital muscular dystrophy: a case report af Elaheh Nekouei, Elmira Shokrolahi Yancheshmeh, Javad Mohammadi-Asl, Zafar Maasoumi Moghaddam

Få fuldtekst

Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family af Farah Talebi, Farideh Ghanbari Mardasi, Javad Mohammadi Asl, Ali Lashgari, Freidoon Farhadi

Få fuldtekst

بررسی پلی‌مورفیسم ژن سوپراکسید دیسموتاز 1 و ارتباط آن با رتینوپاتی و نفروپاتی در بیماران مبتلا به دیابت نوع 2 در اهواز... af Javad Mohammadi-Asl, Arghavan Soleimanizadeh, Hajieh Bibi Shahbazian, Heshmatollah Shahbazian, Neda Golchin

Få fuldtekst

Digenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family af Kourosh Riahi, Farideh Ghanbari Mardasi, Farah Talebi, Farzad Jasemi, Javad Mohammadi Asl

Få fuldtekst

Identification of a Novel WFS1 Mutation Using the Whole Exome Sequencing in an Iranian Pedigree with Autosomal Dominant Hearing Loss af Javad Mohammadi Asl, Nader Saki, Masoud Dehdashtiyan, Mostafa Neissi, Farideh Ghanbari Mardasi

Få fuldtekst