Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 222,879,424 papers from all fields of science
Search
Sign In
Create Free Account
14q32.3
A chromosome band present on 14q
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
6 relations
AKT1 wt Allele
Chromosomes
KLC1 wt Allele
MTA1 wt Allele
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2012
Review
2012
A phenotype map for 14q32.3 terminal deletions
H. Engels
,
H. Schüler
,
+14 authors
H. Reutter
American Journal of Medical Genetics. Part A
2012
Corpus ID: 205315714
Detailed molecular‐cytogenetic studies combined with thorough clinical characterization are needed to establish genotype…
Expand
2005
2005
14q32.3 deletion syndrome with autism
J. Merritt
,
S. Jalal
,
W. Barbaresi
,
D. Babovic‐Vuksanovic
American Journal of Medical Genetics. Part A
2005
Corpus ID: 11128710
Terminal deletions of 14q32.3 are a rare entity with few published cases that have been defined as a specific phenotype [Ortigas…
Expand
2001
2001
Interphase detection of immunoglobulin heavy chain gene translocations with specific oncogene loci in 173 patients with B-cell lymphoma.
A. Tamura
,
I. Miura
,
+8 authors
M. Taniwaki
Cancer Genetics and Cytogenetics
2001
Corpus ID: 44465198
2001
2001
Detection of illegitimate rearrangement within the immunoglobulin locus on 14q32.3 in B‐cell malignancies using end‐sequenced probes
T. Poulsen
,
A. Silahtaroglu
,
+4 authors
H. Johnsen
Genes, Chromosomes and Cancer
2001
Corpus ID: 6308013
Translocation involving the immunoglobulin heavy chain (IGH) locus is a recurring event in B‐cell oncogenesis. The aim of this…
Expand
Review
1999
Review
1999
Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level
J. Barber
,
Carrie Reed
,
C. Joyce
,
S. Dahoun
,
CSophie P. Dahoun
Human Genetics
1999
Corpus ID: 6902450
Abstract Euchromatic imbalances at the cytogenetic level are usually associated with phenotypic consequences. Among the…
Expand
1998
1998
Submicroscopic deletion in 14q32.3 through a de novo tandem translocation between 14q and 21p.
D. Meschede
,
R. Exeler
,
B. Wittwer
,
J. Horst
American journal of medical genetics
1998
Corpus ID: 3219407
We describe a male child with craniofacial anomalies, postnatal onset growth retardation, microcephaly, multiple minor anomalies…
Expand
Review
1997
Review
1997
Delineation of 14q32.3 deletion syndrome.
A. Ortigas
,
C. Stein
,
L. L. Thomson
,
J. Hoo
,
D. Stein
Journal of Medical Genetics
1997
Corpus ID: 1069649
A patient with a 14q32.3 terminal band deletion and cat cry is reported. Review of four other 14q32.3 deletion cases suggests the…
Expand
1991
1991
Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombination.
J. C. Benger
,
I. Teshima
,
M. Walter
,
M. G. Brubacher
,
G. Daouk
,
D. Cox
Genomics
1991
Corpus ID: 30418658
1987
1987
Complex translocation t(8;12;14) in a cell line derived from a child with nonendemic Burkitt-type acute lymphoblastic leukemia.
E. Nacheva
,
P. Fischer
,
+7 authors
H. Gadner
Cancer Genetics and Cytogenetics
1987
Corpus ID: 40347565
Review
1986
Review
1986
A chromosome 14 inversion in a T-cell lymphoma is caused by site-specific recombination between immunoglobulin and T-cell receptor loci
C. Denny
,
Y. Yoshikai
,
T. Mak
,
Stephen D. Smith
,
G. Hollis
,
I. Kirsch
Nature
1986
Corpus ID: 4361783
Specific chromosomal aberrations are associated with specific types of cancer (for review see ref. 1). The distinctiveness of…
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