Sage Journals: Discover world-class research

Free access

First published 1999-12

Should genetic analysis in newborn screening and a heterozygote test for hyperphenylalaninaemia be recommended? An Italian study

Journal of Medical Screening

Retricted access

Research article

First published 2006-12

Heterozygote Carrier Testing in High Schools Abroad: What are the Lessons for the U.S.?

Lainie Friedman Ross

The Journal of Law,Medicine & Ethics

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Research article

First published 2004-06

Heterozygosity for Tay-Sachs and Sandhoff Diseases in Non-Jewish Americans with Ancestry from Ireland,Great Britain,or Italy

Kelly Johnston Branda, Jerzy Tomczak, Marvin R. Natowicz

Genetic Testing and Molecular Biomarkers

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Research article

First published 2006-09

Screening for sickle cell disease on dried blood: a new approach evaluated on 27,000 Belgian newborns

Journal of Medical Screening

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Research article

First published 1997-9

Heterozygosity for Tay-Sachs and Sandhoff Diseases among Massachusetts Residents with French Canadian Background

Elizabeth M Prence, Cheryl A Jerome, Barbara L Triggs-Raine [...]

Journal of Medical Screening

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Other

First published 1997-04

Temporal Changes in the Activated Protein C Resistance Ratio in a Heterozygote for Factor V Leiden Are Abolished by Dilution in Factor V-Deficient Plasma

Todd Meyer, Maria Garcia, Elizabeth Helms [...]

Clinical and Applied Thrombosis/Hemostasis

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Research article

First published 1978-1

Influence of Cystic Fibrotic and Heterozygous Serum on Rat Jejunum 1

J. P. Gilmore, M. Davis, G. E. Gibbs

Experimental Biology and Medicine

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Research article

First published 1992-10

Bovine Plasma β-Mannosidase Activity and Its Potential use for β-Mannosidosis Carrier Detection

Kevin T. Cavanagh, Margaret Z. Jones, Bruce Abbitt [...]

Journal of Veterinary Diagnostic Investigation

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Research article

First published 2000-12

Connexin-26 Gene Analysis in Hearing-Impaired Newborns

Jeff M. Milunsky, Thomas A. Maher, Elif Yosunkaya [...]

Genetic Testing and Molecular Biomarkers

Free access

Research article

First published 1998-03

Hereditary haemochromatosis mutation frequencies in the general population

Journal of Medical Screening

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