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Publications by M. Ansar
A Homozygous Missense Mutation in SLC25A16 Is Associated With Autosomal Recessive Isolated Fingernail Dysplasia in a Pakistani Family
British Journal of Dermatology
Dermatology
Medicine
Flow Estimations Through Spillways Under Submerged Tidal Conditions
Computational Methods and Experimental Measurements XIII
Related publications
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family
Frontiers in Genetics
Genetics
Molecular Medicine
A Novel Missense Mutation in MSX1 Underlies Autosomal Recessive Oligodontia With Associated Dental Anomalies in Pakistani Families
Journal of Human Genetics
Genetics
A Novel Homozygous Missense Mutation in BHLHA9 Causes Mesoaxial Synostotic Syndactyly With Phalangeal Reduction in a Pakistani Family
Human Genome Variation
Biochemistry
Genetics
Molecular Biology
INPP5K Variant Causes Autosomal Recessive Congenital Cataract in a Pakistani Family
Clinical Genetics
Genetics
Autosomal Recessive Woolly Hair With Hypotrichosis Caused by a Novel Homozygous Mutation in theP2RY5gene
Experimental Dermatology
Biochemistry
Dermatology
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
Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss
Zahedan Journal of Research in Medical Sciences
Exome Sequencing Identifies a Novel Missense Variant in RRM2B Associated With Autosomal Recessive Progressive External Ophthalmoplegia
Genome Biology
Whole Exome Sequencing Identifies a Novel Dominant Missense Mutation Underlying Leukonychia in a Pakistani Family
Journal of Human Genetics
Genetics
