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Tandem Repeat Variation
Known as:
VNTR
, Variable Number Tandem Repeat
An inherited polymorphism in eukaryotic DNA that results from variations in the number of tandem repeat nucleotide sequences, which are end-to-end…
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National Institutes of Health
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Related topics
Related topics
2 relations
Minisatellite Repeats
Variable Number of Tandem Repeats
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Suitability of IS6110-RFLP and MIRU-VNTR for Differentiating Spoligotyped Drug-Resistant Mycobacterium tuberculosis Clinical Isolates from Sichuan in China
Chao Zheng
,
Yuding Zhao
,
+9 authors
Qun Sun
BioMed Research International
2014
Corpus ID: 14098478
Genotypes of Mycobacterium tuberculosis complex (MTBC) vary with the geographic origin of the patients and can affect…
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2012
2012
Relationship between Polymorphisms of Angiotensin-converting Enzyme Gene Insertion / Deletion , Endothelial Nitric Oxide Synthase Gene Intron 4 VNTR and Risk for Cervical Cancer
Jun-ge Han
,
Hong Jin
,
+6 authors
Lin Zhang
2012
Corpus ID: 43939841
Background and Aims: Angiotensin-converting enzyme gene (ACE) and endothelial nitric oxide synthase gene (eNOS) have been…
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2009
2009
Population-Based Molecular Epidemiology of Leprosy in Cebu, Philippines
R. Sakamuri
,
M. Kimura
,
+9 authors
V. Vissa
Journal of Clinical Microbiology
2009
Corpus ID: 34943892
ABSTRACT To address the persisting problem of leprosy in Cebu, Philippines, we compiled a database of more than 200 patients who…
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2002
2002
Variable Number Tandem Repeat Polymorphism as a Tool of Chimerism Detection in Allogeneic Stem Cell Transplantation
A. Kamel
,
Ghada I. Mossallam
,
+4 authors
A. Nassar
2002
Corpus ID: 54653113
Background: Allogeneic haematopoeitic stem cell transplantation currently represents the only available therapeutic approach in…
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2002
2002
Early detection of RhD status in pregnancies at risk of hemolytic disease of the newborn
C. Cotorruelo
,
C. Biondi
,
S. G. Borrás
,
R. Monaco
,
A. Racca
Clinical and Experimental Medicine (Testo…
2002
Corpus ID: 22069754
Abstract The aim of this work was to investigate the presence of the RHD gene in fetal cells obtained from amniotic fluid. We…
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1999
1999
Complete DNA sequence and characterization of a 330-kb VNTR-rich region on chromosome 6q27 that is commonly deleted in ovarian cancer.
T. Minaguchi
,
M. Matsushima
,
+6 authors
Y. Nakamura
DNA Research
1999
Corpus ID: 43370578
We report the complete genomic DNA sequence and the characterization of a 330-kb region on chromosome 6q27 that is often deleted…
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1997
1997
Mutation and haplotype analysis of phenylalanine hydroxylase alleles in classical PKU patients from the Czech Republic: identification of four novel mutations.
Libor Kozák
,
M. Blažková
,
+4 authors
Clinical Department
Journal of Medical Genetics
1997
Corpus ID: 12179927
Mutations, haplotypes, and other polymorphic markers in the phenylalanine hydroxylase (PAH) gene were analysed in 133 unrelated…
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1995
1995
AMPFLP analysis of the VNTR loci D1S80 and ApoB in Hungary
J. Woller
,
S. Furedi
,
Z. Pádár
Zeitschrift für Rechtsmedizin
1995
Corpus ID: 7782073
Population data studies for D1S80 and ApoB were carried out on a caucasian population sample from Hungary of 229 and 222…
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1993
1993
Testing independence of fragment lengths within VNTR loci.
S. Geisser
,
Wesley Johnsont
American Journal of Human Genetics
1993
Corpus ID: 38954061
Methods that were devised to test independence of the bivariate fragment lengths obtained from VNTR loci are applied to several…
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1991
1991
Spawning patterns in the three‐spined stickleback (Gasterosteus aculeatus L.): an evaluation by DNA fingerprinting
C. Rico
,
U. Kuhnlein
,
G. J. Fitzgerald
1991
Corpus ID: 53586740
We analysed a random sample of 10 three-spined stickleback nests by DNA fingerprinting. DNA from the guardian male and a random…
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