Sage Journals: Discover world-class research

Retricted access

Research article

First published 1996-10

Possible association between multiple sclerosis and the human T cell leukemia virus (HTLV)-related endogenous element,HRES-I

HB Rasmussen, A Heltberg, K Christensen [...]

Multiple Sclerosis Journal

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Research article

First published 1976-4

Comparison of dy and dy 2J,Two Alleles Expressing Forms of Muscular Dystrophy in the Mouse

A. D. MacPike, Hans Meier

Experimental Biology and Medicine

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Research article

First published 2000-12

The M34T Allele Variant of Connexin 26

Robert A. Cucci, Sai Prasad, Philip M. Kelley [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 1967-11

Genetic Regulation of Multiple Forms of Tyrosinase in Mice

Thomas J. Holstein, Jean B. Burnett, Walter C. Quevedo

Experimental Biology and Medicine

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Research article

First published 1993-07

Mutations in the Arylsulfatase A Gene of Japanese Patients with Metachromatic Leukodystrophy

Yoriyasu Hasegawa, Hiroshi Kawame, Yoshikatsu Eto

DNA and Cell Biology

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Research article

First published 1999-05

Human Fc gamma receptor IIA (FcγRIIA) genotyping and association with systemic lupus erythematosus (SLE) in Chinese and Malays in Malaysia

S N Yap, M E Phipps, M Manivasagar [...]

Lupus

Free access

Review article

First published

PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy –Consequences in Clinical Diagnosis and Genetic Counselling

Pascale Richard, Capucine Trollet, Teresa Gidaro [...]

Journal of Neuromuscular Diseases

Free access

Research article

First published 2016-3

Endothelial Protein C Receptor Gene Variants and Risk of Thrombosis

Georgia Anastasiou, Marianna Politou, Loukianos Rallidis [...]

Clinical and Applied Thrombosis/Hemostasis

Open access

Review article

First published 2010

Clopidogrel: A Pharmacogenomic Perspective on its Use in Coronary Artery Disease

Chris Terpening

Clinical Medicine Insights: Cardiology

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Case report

First published 2011-5

Gaucher Disease with Prenatal Onset and Perinatal Death Due to Compound Heterozygosity for the Missense R131C and Null Rec Nci I GBA Mutations

April Goebl, Raechel A. Ferrier, Patrick Ferreira [...]

Pediatric and Developmental Pathology

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