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First published 2015

Phenylalanine and Tyrosine Metabolism Analysis in Heterozygotes for Phenylketonuria and in Healthy Individuals

Roseani Andrade, Vaneisse Monteiro, Cléber Cruz [...]

Journal of Inborn Errors of Metabolism and Screening

Free access

Research article

First published 2014-3

Lipoprotein lipase activity in heterozygotes for lipoprotein lipase gene mutations reveals a gender bias

Toshio Murase, Tetsu Ebara, Minoru Okubo

Annals of Clinical Biochemistry: International Journal of Laboratory Medicine

Retricted access

Research article

First published 1994-09

Prenatal Counseling in Heterozygotes for Ornithine Transcarbamylase Deficiency

Melissa H. Fries, Jeffrey A. Kuller, Elaina Jurecki [...]

Clinical Pediatrics

Open access

Research article

First published 2021

Postpartum Hemorrhage in Heterozygote Factor XIII Deficient Women Compared With Healthy Women. A Cross-Sectional Experience From Iran

Majid Naderi, Ilia Mirzaei, Saeedeh Yaghoubi [...]

Clinical and Applied Thrombosis/Hemostasis

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 2001-09

A Pilot Survey of Cystic Fibrosis Clinical Manifestations in CFTR Mutation Heterozygotes

C. Castellani, C. Quinzii, S. Altieri [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Brief report

First published 2003-06

Connexin-30 Deletion Analysis in Connexin-26 Heterozygotes

Victoria A. Stevenson, Masamichi Ito, Jeff M. Milunsky

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 1965-3

Heterozygosity and Homozygosity in von Willebrand's Disease. ∗

Emily M. Barrow, C. C. Heindel, Harold R. Roberts [...]

Experimental Biology and Medicine

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Other

First published 1972-06

The Detection of the Heterozygote and Homozygote in Cystic Fibrosis by Short Term Lymphocyte Culture Studies: A Defect in RNA Methylation

Owen M. Rennert, Jaime L. Frias, Richard L. Julius [...]

Clinical Pediatrics

Retricted access

Research article

First published 1999-1

Fine Mapping of Progressive Pseudorheumatoid Dysplasia: A Tool for Heterozygote Identification

Asem Alkbateeb, Jamil Al-Alami, Suzanne M. Leal [...]

Genetic Testing and Molecular Biomarkers

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