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13q32
A chromosome band present on 13q.
National Institutes of Health
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Related topics
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4 relations
13q
ABCC4 wt Allele
Chromosomes
DCT wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34
M. Mimaki
,
T. Shiihara
,
+7 authors
M. Mizuguchi
Brain & development (Tokyo. )
2015
Corpus ID: 41057666
2012
2012
Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineated
E. Chabchoub
,
D. Willekens
,
J. Vermeesch
,
J. Fryns
Clinical Genetics
2012
Corpus ID: 33700100
Chabchoub E, Willekens D, Vermeesch JR, Fryns J‐P. Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological…
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2005
2005
Genetic linkage of systemic lupus erythematosus to 13q32 in African American families with affected male members
C. Xing
,
C. Gray‐McGuire
,
+4 authors
J. Olson
Human Genetics
2005
Corpus ID: 10377698
Systemic lupus erythematosus (SLE) is a complex autoimmune disorder involving genetic and environmental factors. Previously, our…
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2004
2004
The KPNB3 locus is associated with schizophrenia
Jun Wei
,
G. Hemmings
Neuroscience Letters
2004
Corpus ID: 21304247
2001
2001
Localisation of a novel region of recurrent amplification in follicular lymphoma to an approximately 6.8 Mb region of 13q32-33.
M. Neat
,
N. Foot
,
+7 authors
J. Fitzgibbon
Genes, Chromosomes and Cancer
2001
Corpus ID: 39707469
Follicular lymphoma (FL) is characterised by the presence of the t(14;18)(q32;q21) and represents approximately 25% of new cases…
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1999
1999
Two distinct regions of deletion on chromosome 13q in primary nasopharyngeal carcinoma
Y. Tsang
,
K. Lo
,
+4 authors
Dolly P. Huang
International Journal of Cancer
1999
Corpus ID: 42198621
Nasopharyngeal carcinoma (NPC) is rare in most parts of the world, but prevalent in Southern China. Although this disease poses a…
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1999
1999
On the Future of Genetic Research in Bipolar and Schizophrenic Syndromes
W. Berrettini
Neuropsychopharmacology
1999
Corpus ID: 33714705
1986
1986
The gene for clotting factor 10 is mapped to 13q32----qter.
N. Royle
,
M. Fung
,
R. MacGillivray
,
J. Hamerton
Cytogenetics and Cell Genetics
1986
Corpus ID: 46739502
The structural gene for the human clotting factor 10 (F10) has been mapped to chromosome 13 with a cDNA probe hybridized to DNAs…
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1985
1985
Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32----qter.
S. Al‐Awadi
,
A. Teebi
,
T. Sundareshan
Annales de Genetique
1985
Corpus ID: 10772010
A five-year-old boy with speech delay, minor facial abnormalities and borderline psychomotor retardation was found to have a…
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1973
1973
Nonrandom distribution of chromosome breaks in Fanconi's anemia.
H. Koskull
,
Pertti Aula
Cytogenetics and Cell Genetics
1973
Corpus ID: 3268216
Fanconi’s anemia is characterized by an increased amount of chromosome breaks. The distribution of the breaks in the human…
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