Discover open access scientific publications

Search, annotate, share and cite publications

Publications by W E Bradley

Model Involving Gene Inactivation in the Generation of Autosomal Recessive Mutants in Mammalian Cells in Culture.

Molecular and Cellular Biology

Molecular Biology

English

Related publications

Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss

Zahedan Journal of Research in Medical Sciences

English

Molecular Analysis of DMP1 Mutants Causing Autosomal Recessive Hypophosphatemic Rickets

English

Mutations in the Nebulin Gene Associated With Autosomal Recessive Nemaline Myopathy

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

GPR126 : A Novel Candidate Gene Implicated in Autosomal Recessive Intellectual Disability

American Journal of Medical Genetics, Part A

English

Newly Discovered Mutations in the GALNT3 Gene Causing Autosomal Recessive Hyperostosis-Hyperphosphatemia Syndrome

Acta Orthopaedica

Sports Medicine

English

Aberrant Smad3 Phosphoisoforms in Cyst-Lining Epithelial Cells in the CPK Mouse, a Model of Autosomal Recessive Polycystic Kidney Disease

American Journal of Physiology - Renal Physiology

English

Bi-Allelic Inactivating Variants in the COCH Gene Cause Autosomal Recessive Prelingual Hearing Impairment

European Journal of Human Genetics

English

Synchronized Mammalian Cells in Suspension Culture

English

Founder Mutations in the Lipase H Gene in Families With Autosomal Recessive Woolly Hair/Hypotrichosis

Journal of Investigative Dermatology

Molecular Biology

English