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Publications by Wasim Ahmad
A Novel Heterozygous Intragenic Sequence Variant in DLX6 Probably Underlies First Case of Autosomal Dominant Split-Hand/Foot Malformation Type 1
Molecular Syndromology
Genetics
Homozygous Sequence Variants in the WNT10B Gene Underlie Split Hand/Foot Malformation
Genetics and Molecular Biology
Genetics
Molecular Biology
Identification of Novel LEPR Mutations in Pakistani Families With Morbid Childhood Obesity
BMC Medical 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
A NovelESRRBDeletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment Among Pakistani Families
Genetics Research International
Genetics
Molecular Biology
Screening, Diagnosis and Genetic Study of Breast Cancer Patients in Pakistan
Pakistan Journal of Medical Sciences
Medicine
Validation of the Mizaj of Heart by Determining the Ash Value of Vital Organs of Three Species
Medical Journal of Islamic World Academy of Sciences
5G: Disruption in Media and Entertainment
Exposing the Human Nude Phenotype
Nature
Multidisciplinary
Noncoding Mutations of HGF Are Associated With Nonsyndromic Hearing Loss, DFNB39
American Journal of Human Genetics
Genetics
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