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21q
Known as:
Chromosome 21 Distal Arm
, Chromosome 21 Long Arm
Distal (long) arm of chromosome 21
National Institutes of Health
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Related topics
Related topics
10 relations
21q11.2
21q21.2
21q21.3
21q22.1
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2007
Highly Cited
2007
Array CGH identifies distinct DNA copy number profiles of oncogenes and tumor suppressor genes in chromosomal- and microsatellite-unstable sporadic colorectal carcinomas
S. Lassmann
,
R. Weis
,
+4 authors
M. Werner
Journal of molecular medicine
2007
Corpus ID: 2956635
DNA copy number changes represent molecular fingerprints of solid tumors and are as such relevant for better understanding of…
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2006
2006
Molecular cytogenetic profiling of complex karyotypes in primary myelodysplastic syndromes and acute myeloid leukemia.
D. Trost
,
B. Hildebrandt
,
M. Beier
,
Nicola Müller
,
U. Germing
,
B. Royer-Pokora
Cancer Genetics and Cytogenetics
2006
Corpus ID: 36159745
2004
2004
Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia.
S. Casas
,
A. Aventín
,
+12 authors
J. Sierra
Cancer Genetics and Cytogenetics
2004
Corpus ID: 41534383
2002
2002
First Evidence of Genetic Imbalances in Angiofibromas
B. Schick
,
C. Brunner
,
M. Praetorius
,
P. Plinkert
,
S. Urbschat
The Laryngoscope
2002
Corpus ID: 20820774
Objective/Hypothesis Angiofibromas are clinically well characterized by their origin at the posterior lateral nasal wall close to…
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Highly Cited
2002
Highly Cited
2002
Chromosomal imbalances of primary and metastatic lung adenocarcinomas
A. Goeze
,
K. Schlüns
,
Guenter Wolf
,
Zsuzsanna Thäsler
,
S. Petersen
,
I. Petersen
Journal of Pathology
2002
Corpus ID: 22411776
Comparative genomic hybridization (CGH) was used to screen 83 lung adenocarcinomas of 60 patients for chromosomal imbalances. The…
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2001
2001
Genetic abnormalities specifically associated with varying metastatic potential of prostate cancer cell lines as detected by comparative genomic hybridization.
L. Chu
,
C. Pettaway
,
J. Liang
Cancer Genetics and Cytogenetics
2001
Corpus ID: 36575306
1996
1996
Isochromosomes in acute lymphoblastic leukaemia: I(21q) is a significant finding
M. Martineau
,
Roslyn Clark
,
Dianna M. Farrell
,
J. Hawkins
,
A. Moorman
,
L. Secker-Walker
Genes, Chromosomes and Cancer
1996
Corpus ID: 23696687
The incidence, type, and clonality of isochromosomes at diagnosis were investigated in acute lymphoblastic leukaemia (ALL). An…
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1996
1996
Cytogenetic and clinicobiological features of acute leukemia with stem cell phenotype: study of nine cases.
A. Cuneo
,
A. Ferrant
,
+9 authors
H. van den Berghe
Cancer Genetics and Cytogenetics
1996
Corpus ID: 45786304
1995
1995
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.
J. Blouin
,
Derek H. Christie
,
+5 authors
S. Antonarakis
American Journal of Human Genetics
1995
Corpus ID: 28124223
We have used a half-YAC containing the human chromosome 21 long-arm telomere to clone, map, and characterize a new dinucleotide…
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Highly Cited
1990
Highly Cited
1990
Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations.
S. Antonarakis
,
P. A. Adelsberger
,
M. Petersen
,
F. Binkert
,
A. Schinzel
American Journal of Human Genetics
1990
Corpus ID: 40281457
Down syndrome is rarely due to a de novo duplication of chromosome 21 [dup(21q)]. To investigate the origin of the dup(21q) and…
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