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Heterozygote Detection

Known as: Genetic Carrier, Detection, Detections, Heterozygote, Carriers, Genetic, Detection 
Identification of genetic carriers for a given trait.
National Institutes of Health

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3 relations
Genetic Screening (procedure)Genetic screening methodHeterozygote

Papers overview

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Highly Cited
2020
Highly Cited
2020
ABO histo-blood groups influence gut microbiome, with causal relationship between Bacteroides and inflammatory bowel disease
The intestinal microbiome is implicated as an important modulating factor in multiple inflammatory neurologic and neoplastic… 
2011
2011
Coexisting/Coexpressing Genomic Libraries (CoGeL) identify interactions among distantly located genetic loci for developing complex microbial phenotypes
In engineering novel microbial strains for biotechnological applications, beyond a priori identifiable pathways to be engineered… 
Highly Cited
2008
Highly Cited
2008
Demonstration of rapid multiplex PCR amplification involving 16 genetic loci.
2002
2002
Identification of a novel NCF-1 (p47-phox) pseudogene not containing the signature GT deletion: significance for A47 degrees chronic granulomatous disease carrier detection.
The p47-phox gene, NCF-1, has 2 nearly identical pseudogenes (psiNCF-1) in proximity at chromosomal locus 7q11.23. A dinucleotide… 
Highly Cited
1998
Highly Cited
1998
Analysis of multiplexed short tandem repeat (STR) systems using capillary array electrophoresis
The profiling of polymorphic short tandem repeat (STR) markers is being applied to human identification, parentage testing and… 
Highly Cited
1995
Highly Cited
1995
An investigation of whether polymorphisms of cytochrome P4502E1 are genetic markers of susceptibility to alcoholic end‐stage organ damage in a chinese population
The human cytochrome P4502E1 gene (P4502E1), coding for an ethanol‐inducible nitrosamine‐metabolizing P‐450, is involved in the… 
1984
1984
CARRIER DETECTION BY DIRECT GENE ANALYSIS IN A FAMILY WITH HAEMOPHILIA B (FACTOR IX DEFICIENCY)
Highly Cited
1979
Highly Cited
1979
Genetic polymorphism in normal human fibroblasts as analyzed by two-dimensional polyacrylamide gel electrophoresis.
Highly Cited
1976
Highly Cited
1976
Carrier detection in Duchenne muscular dystrophy.
We measured endogenous phosphorylation of peak II (apparent molecular weight of 220,000 daltons) of the erythrocyte membrane in… 
Highly Cited
1970
Highly Cited
1970
Carrier detection in Duchenne muscular dystrophy. A comparative study of electron microscopy, light microscopy and serum enzymes.
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