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Publications by Anam Hammid

A Novel Heterozygous Intragenic Sequence Variant in DLX6 Probably Underlies First Case of Autosomal Dominant Split-Hand/Foot Malformation Type 1

Molecular Syndromology

English

Related publications

Homozygous Sequence Variants in the WNT10B Gene Underlie Split Hand/Foot Malformation

Genetics and Molecular Biology

Molecular Biology

English

Absent Expression of the Osteoblast-Specific Maternally Imprinted Genes,DLX5andDLX6,causes Split Hand/Split Foot Malformation Type I

Journal of Medical Genetics

English

Bilateral Split Hand and Split Foot Malformation in a Boy With a De Novo Interstitial Deletion of 7q21.3

Journal of Medical Genetics

English

A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness

BioMed Research International

Molecular Biology

English

Rare Missense Variant p.Ala505Ser in the ZAK Protein Observed in a Patient With Split-Hand/Foot Malformation From a Non-Consanguineous Pedigree

Journal of International Medical Research

English

A Novel Heterozygous Mutation in Cardiac Calsequestrin Causes Autosomal Dominant Catecholaminergic Polymorphic Ventricular Tachycardia

Cardiovascular Medicine

English

Recurrent Streptococcus Pneumoniae Meningitis in a Child With Split Hand and Foot Malformation and Undiagnosed Mondini Dysplasia

Journal of Developmental and Physical Disabilities

Physical Therapy

Educational Psychology

English

Novel Heterozygous C243Y A20/Tnfaip3 Gene Mutation Is Responsible for Chronic Inflammation in Autosomal-Dominant Behçet's Disease

English

A Case of Autosomal Dominant Osteopetrosis Type II With a CLCN7 Gene Mutation

JCRPE Journal of Clinical Research in Pediatric Endocrinology

English