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Publications by Naveed Altaf Malik
Novel Missense Mutation in the RSPO4 Gene in Congenital Hyponychia and Evidence for a Polymorphic Initiation Codon (p.M1I)
BMC Medical Genetics
Genetics
Related publications
A Novel Missense Mutation of F 9 Gene in Hemophilia B Patients
Journal of Blood Disorders & Transfusion
A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia
Reproductive Sciences
Gynecology
Obstetrics
Creutzfeldt-Jakob Disease Associated With a Missense Mutation at Codon 200 of the Prion Protein Gene in Brazil
Dementia e Neuropsychologia
Gerontology
Geriatrics
Neurology
Sensory Systems
Cognitive Neuroscience
An Initiation Codon Mutation (AUG----GUG) of the Human Alpha 1-Globin Gene. Structural Characterization and Evidence for a Mild Thalassemic Phenotype.
Journal of Clinical Investigation
Medicine
A Novel Missense Mutation T101N in the Melanocortin-4 Receptor Gene Associated With Obesity
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
Affected Siblings With Alzheimer's Disease Had Missense Mutation of Codon 717 in Amyloid Precursor Protein Gene.
Japanese Journal of Geriatrics
Gerontology
Geriatrics
A Novel Missense Mutation in the CYLD Gene in a Spanish Family With Multiple Familial Trichoepithelioma
Archives of Dermatology
A Novel Missense Mutation p.L76P in the GJB2 Gene Causing Nonsyndromic Recessive Deafness in a Brazilian Family
Brazilian Journal of Medical and Biological Research
Immunology
Cell Biology
Pharmacology
Biochemistry
Biophysics
Neuroscience
Medicine
Toxicology
Physiology
Pharmaceutics
A Novel Missense Mutation That May Be Associated With the Polydactyly in the HOXD13 Gene: Q241H
The Annals of Clinical and Analytical Medicine
