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2q21
A chromosome band present on 2q
National Institutes of Health
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Related topics
Related topics
5 relations
CXCR4 wt Allele
Chromosomes
ERCC3 wt Allele
GPR17 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
Loss of heterozygosity at 19p13.2 and 2q21 in tumours from familial clusters of non-medullary thyroid carcinoma
H. Prazeres
,
F. Rodrigues
,
+5 authors
T. Martins
Familial Cancer
2007
Corpus ID: 7531181
Linkage studies have identified susceptibility loci for familial nonmedullary thyroid cancer (FNMTC), with and without cell…
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2007
2007
Fine deletion mapping of chromosome 2q21-37 shows three preferentially deleted regions in oral cancer.
B. Cengiz
,
M. Gunduz
,
+9 authors
N. Nagai
Oral Oncology
2007
Corpus ID: 37012427
Review
2004
Review
2004
Detection of an interstitial deletion of 2q21‐22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocation
A. Shanske
,
L. Edelmann
,
N. Kardon
,
P. Gosset
,
B. Levy
American Journal of Medical Genetics. Part A
2004
Corpus ID: 23518101
Various molecular cytogenetic techniques are currently available to accurately characterize chromosome rearrangements in patients…
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Review
2004
Review
2004
Pericentric inversions in man: personal experience and review of the literature
A. Kleczkowska
,
J. Fryns
,
H. Berghe
Human Genetics
2004
Corpus ID: 24145314
SummaryThe Leuven cytogenetic centre experience on pericentric inversion in man is discussed with exclusion of the pericentric…
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2001
2001
Genetic events during the transformation of a tamoxifen-sensitive human breast cancer cell line into a drug-resistant clone.
R. Achuthan
,
S. Bell
,
+5 authors
V. Speirs
Cancer Genetics and Cytogenetics
2001
Corpus ID: 24439047
2001
2001
Generalized epilepsy with febrile seizures plus
H. Lerche
,
Y. Weber
,
+5 authors
F. Lehmann‐Horn
Neurology
2001
Corpus ID: 29147252
Background: Generalized epilepsy with febrile seizures plus (GEFS+) is a recently described benign childhood-onset epileptic…
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2001
2001
Identification of novel deletion regions on chromosome arms 2q and 6p in breast carcinomas by amplotype analysis
Z. Piao
,
Kyong-Sik Lee
,
Hoguen Kim
,
M. Perucho
,
S. Malkhosyan
Genes, Chromosomes and Cancer
2001
Corpus ID: 25204608
DNA fingerprinting by arbitrarily primed PCR (AP‐PCR) was employed to identify molecular genetic alterations in 37 primary breast…
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Highly Cited
1994
Highly Cited
1994
cDNA cloning and chromosomal mapping of human N-acetylglucosaminyltransferase V+.
Hiroyuki Saito
,
Atsushi Nishikawa
,
+6 authors
Naoyuki Taniguchi
Biochemical and Biophysical Research…
1994
Corpus ID: 39553522
Human N-acetylglucosaminyltransferase V (GnT-V, EC 2.4.1.155) cDNA was isolated from a human fetal liver cDNA library…
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Highly Cited
1993
Highly Cited
1993
Regional localization of the lactase‐phlorizin hydrolase gene, LCT, to chromosome 2q21
C. Harvey
,
M. Fox
,
P. Jeggo
,
N. Mantei
,
S. Povey
,
D. Swallow
Annals of Human Genetics
1993
Corpus ID: 38604778
The gene LCT which codes for the intestinal disaccharidase lactase‐phlorizin hydrolase has previously been mapped, using somatic…
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1991
1991
Chromosomal characterizations of human nasal and nasopharyngeal cells immortalized by human papillomavirus type 16 DNA.
Maria Dȩbiec-Rychter
,
Kim Zukowski
,
Ching Y. Wang
,
Wu-Nan Wen
Cancer Genetics and Cytogenetics
1991
Corpus ID: 30615232
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