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14q32.3
A chromosome band present on 14q
National Institutes of Health
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6 relations
AKT1 wt Allele
Chromosomes
KLC1 wt Allele
MTA1 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
From Genotypes of Immunoglobulin Constant Heavy G Chains (Fcγ) (GM) Genes (IGHG) to Phenotypes in Childhood Asthma
V. Oxelius
International Archives of Allergy and Immunology
2012
Corpus ID: 25454393
Background: IgE-mediated allergy is associated with immunoglobulin heavy constant G chain (Fcγ) (GM) genes (IGHG) on chromosome…
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2001
2001
Assignment1 of the human metastasis-associated gene 1 (MTA1) to human chromosome band 14q32.3 by fluorescence in situ hybridization
Q. Cui
,
S. Takiguchi
,
K. Matsusue
,
Y. Toh
,
M. Yoshida
Cytogenetic and Genome Research
2001
Corpus ID: 46477197
Fig. 1. FISH of a digoxigenin-labeled MTA1 probe to normal human chromosomes. Double signals were detected at region q32.3 on…
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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…
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1999
1999
Fluorescence in situ hybridization analysis shows the frequent occurrence of 14q32.3 rearrangements with involvement of immunoglobulin switch regions in myeloma cell lines.
Jeroen Kuipers
,
J. Vaandrager
,
+5 authors
Bert J. E. G. Bast
Cancer Genetics and Cytogenetics
1999
Corpus ID: 6084261
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…
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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…
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1995
1995
Intermediate lymphocytic lymphoma with both t(14;19)(q32.3;q13.1) and t(3;22)(q27;q11.2).
M. Nakagawa
,
H. Sugiyama
,
+7 authors
T. Kishimoto
Cancer Genetics and Cytogenetics
1995
Corpus ID: 988144
1992
1992
Mapping of the gene family for human heat-shock protein 90 alpha to chromosomes 1, 4, 11, and 14.
K. Ozawa
,
Y. Murakami
,
T. Eki
,
E. Soeda
,
K. Yokoyama
Genomics
1992
Corpus ID: 25330272
The HSP90 family of heat-shock proteins (encoded by genes for HSP90 alpha and beta) constitutes one of the major groups of…
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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
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