Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,256,227 papers from all fields of science
Search
Sign In
Create Free Account
chromosome 14q
Known as:
14q
, Chromosome 14 Distal Arm
, Chromosome 14 Long Arm
Distal (long) arm of chromosome 14
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
39 relations
14q11
14q11.1-q11.2
14q11.2
14q11.2-q12
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2002
Review
2002
Further delineation of the chromosome 14q terminal deletion syndrome.
C. V. van Karnebeek
,
Safira Quik
,
S. Sluijter
,
M. Hulsbeek
,
J. Hoovers
,
R. Hennekam
American journal of medical genetics
2002
Corpus ID: 7342531
A patient with hypotonia, blepharophimosis, ptosis, a bulbous nose, a long philtrum, upturned corners of the mouth, and mild…
Expand
Highly Cited
2002
Highly Cited
2002
Detection of genetic alterations in advanced prostate cancer by comparative genomic hybridization.
K. Kasahara
,
T. Taguchi
,
I. Yamasaki
,
M. Kamada
,
K. Yuri
,
T. Shuin
Cancer Genetics and Cytogenetics
2002
Corpus ID: 20107288
2002
2002
Chromosome 14q LOH in localized clear cell renal cell carcinoma
K. Mitsumori
,
John M. Kittleson
,
+5 authors
A. Reeve
Journal of Pathology
2002
Corpus ID: 2934843
The progression of a malignant tumour is understood to be the result of the accumulation of multiple genetic aberrations. As up…
Expand
Highly Cited
2001
Highly Cited
2001
Comparative genomic hybridization of esophageal squamous cell carcinoma
C. Yen
,
Yann-Jang Chen
,
+7 authors
Chi-Hung Lin
Cancer
2001
Corpus ID: 24328741
Esophageal carcinoma is a major cause of cancer‐related deaths among males in Taiwan. However, to date, the genetic alterations…
Expand
Highly Cited
1997
Highly Cited
1997
Recurrent DNA copy number changes in 1q, 4q, 6q, 9p, 13q, 14q and 22q detected by comparative genomic hybridization in malignant mesothelioma.
Anna‐Maria Björkqvist
,
L. Tammilehto
,
S. Anttila
,
K. Mattson
,
S. Knuutila
British Journal of Cancer
1997
Corpus ID: 849980
Comparative genomic hybridization (CGH) analyses were performed on 27 human pleural mesothelioma tumour specimens, consisting of…
Expand
Highly Cited
1997
Highly Cited
1997
Significance of chromosome arm 14q loss in nonpapillary renal cell carcinomas
J. Herbers
,
D. Schullerus
,
+5 authors
G. Kovacs
Genes, Chromosomes and Cancer
1997
Corpus ID: 24899588
We examined 88 nonpapillary renal cell carcinomas for allelic loss at chromosome arm 14q and correlated the results to size…
Expand
Highly Cited
1995
Highly Cited
1995
Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.
Suzana Gispert
,
'. N. Santos
,
+7 authors
'. GeorgAuburger
American Journal of Human Genetics
1995
Corpus ID: 42963857
Three large pedigrees of German descent with autosomal dominant "pure" familial spastic paraplegia (FSP) were characterized…
Expand
1990
1990
Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas.
M. Nilbert
,
N. Mandahl
,
+5 authors
F. Mitelman
Cancer Genetics and Cytogenetics
1990
Corpus ID: 45910479
Review
1979
Review
1979
Trisomy 14 mosaicism: case report and review.
V. P. Johnson
,
T. Aceto
,
C. Likness
American journal of medical genetics
1979
Corpus ID: 41867813
Complete or partial trisomy 14 is compatible with life. However, in the former case, mosaicism is probably always present. A case…
Expand
Highly Cited
1977
Highly Cited
1977
Chromosome 14 translocation in african and north american burkitt's lymphoma
B. Kaiser‐Mccaw
,
A. Epstein
,
H. Kaplan
,
F. Hecht
International Journal of Cancer
1977
Corpus ID: 33060886
Two established North American Burkitt lymphoma cell lines were studied by chromosomal banding techniques. The SU‐AmB‐1 line…
Expand
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