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Publications by Obaid Ur Rahman

Deletion Mutation in BSCL2 Gene Underlies Congenital Generalized Lipodystrophy in a Pakistani Family

Diagnostic Pathology

Forensic Medicine

English

Related publications

Congenital Generalized Lipodystrophy

Jornal de Pediatria

English

Exogenous Insulin Ameliorates Acanthosis Nigricans in Congenital Generalized Lipodystrophy

Pediatric Research

English

Type 2 Congenital Generalized Lipodystrophy: The Diagnosis Is in Your Hands

Journal of Pediatrics

English

The Human Lipodystrophy Gene BSCL2/Seipin May Be Essential for Normal Adipocyte Differentiation

Internal Medicine

English

Aggressive Papillary Thyroid Carcinoma in a Child With Type 2 Congenital Generalized Lipodystrophy

Archives of endocrinology and metabolism

English

INPP5K Variant Causes Autosomal Recessive Congenital Cataract in a Pakistani Family

Clinical Genetics

English

A Novel Splicing Mutation in the FBN2 Gene in a Family With Congenital Contractural Arachnodactyly

Frontiers in Genetics

Molecular Medicine

English

A Novel Missense Mutation in MSX1 Underlies Autosomal Recessive Oligodontia With Associated Dental Anomalies in Pakistani Families

Journal of Human Genetics

English

Generalized Lipodystrophy

English