Molecular Genetics of Common and Complex Disease

Pub Date A-Z
Peroxisome Biogenesis Disorders
Yukio Fujiki
Published online: May 2011
Osteoporosis: Genetics
Wen‐Feng Li, Shu‐Xun Hou, Claude Férec, Jian‐Min Chen
Published online: April 2011
Genetics of Glaucoma
Yutao Liu, R Rand Allingham
Published online: December 2010
Neural Tube Defects: Genetics
Michelle R O'Byrne, Kit Sing Au, Hope Northrup
Published online: November 2010
DNA Repair: Disorders
Alan R Lehmann, Mark O'Driscoll
Published online: October 2010
Legius Syndrome and SPRED1
Hilde Brems, Thomy de Ravel, Eric Legius
Published online: October 2010
Non‐B DNA Structure and Mutations Causing Human Genetic Disease
Albino Bacolla, David N Cooper, Karen M Vasquez
Published online: October 2010
Gastric Cancer
Karl‐Friedrich Becker, Gisela Keller
Published online: October 2010
MicroRNAs and Human Disease
Christian Marin‐Muller, Qizhi Yao, Changyi Chen
Published online: October 2010
Gap Junctions and Connexins: The Molecular Genetics of Deafness
Regina Nickel, Andrew Forge
Published online: October 2010
Epilepsy: Genetics
Kate V Everett
Published online: October 2010
Ion Channels and Human Disorders
Dipa L Raja Rayan, Michael G Hanna
Published online: October 2010
Molecular Genetics of Hereditary Spastic Paraplegias
Giovanni Stevanin
Published online: September 2010
Research on Rare Variants for Complex Diseases
Chee Seng Ku, Patrik KE Magnusson, Kee Seng Chia, Yudi Pawitan
Published online: September 2010
Modifier Genes in the Haemoglobinopathies
Rosalba Di Marzo, Roberta Calzolari, Deborah Rund, Aurelio Maggio
Published online: September 2010
Molecular Genetics of Type 1 Diabetes
Yi Ye, Kay L Mehers, Kathleen M Gillespie
Published online: September 2010
Molecular Genetics of Cardiovascular Disease
Wai Kwong Lee, Sandosh Padmanabhan, Anna F Dominiczak
Published online: September 2010
Genetics of Retinal Disease
Peter J Francis
Published online: September 2010
Nonsense Mutations Causing Inherited Diseases: Therapeutic Approaches
Laure Bidou, Valérie Allamand
Published online: September 2010
22q11 Deletion Syndrome: A Role for Tbx1 in Pharynx and Cardiovascular Development
Amelie Calmont, Peter Scambler
Published online: September 2010
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