Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 227,143,987 papers from all fields of science
Search
Sign In
Create Free Account
Heterozygote Detection
Known as:
Genetic Carrier, Detection
, Detections, Heterozygote
, Carriers, Genetic, Detection
Expand
Identification of genetic carriers for a given trait.
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
3 relations
Genetic Screening (procedure)
Genetic screening method
Heterozygote
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2020
Highly Cited
2020
ABO histo-blood groups influence gut microbiome, with causal relationship between Bacteroides and inflammatory bowel disease
M. Rühlemann
,
B. Hermes
,
+20 authors
A. Franke
medRxiv
2020
Corpus ID: 231641761
The intestinal microbiome is implicated as an important modulating factor in multiple inflammatory neurologic and neoplastic…
Expand
2011
2011
Coexisting/Coexpressing Genomic Libraries (CoGeL) identify interactions among distantly located genetic loci for developing complex microbial phenotypes
Sergios A. Nicolaou
,
S. Gaida
,
E. Papoutsakis
Nucleic Acids Research
2011
Corpus ID: 8725580
In engineering novel microbial strains for biotechnological applications, beyond a priori identifiable pathways to be engineered…
Expand
Highly Cited
2008
Highly Cited
2008
Demonstration of rapid multiplex PCR amplification involving 16 genetic loci.
P. Vallone
,
C. Hill
,
J. Butler
Forensic Science International: Genetics
2008
Corpus ID: 13709312
Highly Cited
2003
Highly Cited
2003
A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21
A. Rajab
,
G. Mochida
,
+6 authors
C. Walsh
Neurology
2003
Corpus ID: 17241021
Objective: To describe a novel form of pontocerebellar hypoplasia (PCH) and map its genetic locus. Background: PCH is a…
Expand
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.
P. Heyworth
,
D. Noack
,
A. Cross
Blood
2002
Corpus ID: 41556810
The p47-phox gene, NCF-1, has 2 nearly identical pseudogenes (psiNCF-1) in proximity at chromosomal locus 7q11.23. A dinucleotide…
Expand
Highly Cited
1998
Highly Cited
1998
Analysis of multiplexed short tandem repeat (STR) systems using capillary array electrophoresis
E. Mansfield
,
J. Robertson
,
+9 authors
B. McCord
Electrophoresis
1998
Corpus ID: 25607287
The profiling of polymorphic short tandem repeat (STR) markers is being applied to human identification, parentage testing and…
Expand
1984
1984
CARRIER DETECTION BY DIRECT GENE ANALYSIS IN A FAMILY WITH HAEMOPHILIA B (FACTOR IX DEFICIENCY)
I. Peake
,
B. Furlong
,
A. Bloom
The Lancet
1984
Corpus ID: 35737702
Highly Cited
1979
Highly Cited
1979
Genetic polymorphism in normal human fibroblasts as analyzed by two-dimensional polyacrylamide gel electrophoresis.
K. E. Walton
,
D. Styer
,
E. Gruenstein
Journal of Biological Chemistry
1979
Corpus ID: 8579202
Highly Cited
1976
Highly Cited
1976
Carrier detection in Duchenne muscular dystrophy.
A. Roses
,
M. Roses
,
S. Miller
,
Keith L. Hull
,
S. Appel
New England Journal of Medicine
1976
Corpus ID: 27552306
We measured endogenous phosphorylation of peak II (apparent molecular weight of 220,000 daltons) of the erythrocyte membrane in…
Expand
Highly Cited
1970
Highly Cited
1970
Carrier detection in Duchenne muscular dystrophy. A comparative study of electron microscopy, light microscopy and serum enzymes.
S. Roy
,
V. Dubowitz
Journal of Neurological Sciences
1970
Corpus ID: 70939194
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE