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Publications by Syed Muhammad Jamal
Localization of a Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus (DFNB38) to 6q26-Q27 in a Consanguineous Kindred From Pakistan
Human Heredity
Genetics
Related publications
Mutation of COL11A2 Causes Autosomal Recessive Non-Syndromic Hearing Loss at the DFNB53 Locus
Journal of Medical Genetics
Genetics
DFNB20: A Novel Locus for Autosomal Recessive, Non-Syndromal Sensorineural Hearing Loss Maps to Chromosome 11q25–qter
European Journal of Human Genetics
Genetics
Novel Mutations Confirm That COL11A2 Is Responsible for Autosomal Recessive Non-Syndromic Hearing Loss DFNB53
Molecular Genetics and Genomics
Medicine
Genetics
Molecular Biology
Identification of a Novel Homozygous Mutation, TMPRSS3: C.535G>A, in a Tibetan Family With Autosomal Recessive Non-Syndromic Hearing Loss
PLoS ONE
Multidisciplinary
Genotype-Phenotype Correlation Analysis of MYO15A Variants in Autosomal Recessive Non-Syndromic Hearing Loss
BMC Medical Genetics
Genetics
Autosomal Recessive Primary Generalized Dystonia in Two Siblings From a Consanguineous Family
Movement Disorders
Neurology
Genome-Wide Analysis Reveals a Novel Autosomal-Recessive Hearing Loss Locus DFNB80 on Chromosome 2p16.1-P21
Journal of Human Genetics
Genetics
A NovelESRRBDeletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment Among Pakistani Families
Genetics Research International
Genetics
Molecular Biology
Insight to FBXO31 Novel Mutation p.Cys283Asn Causing Non‑Syndromic Autosomal Recessive Intellectual Disability Using Computational Methods
Clinical Proteomics and Bioinformatics
