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14q31.1
A chromosome band present on 14q
National Institutes of Health
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2 relations
Chromosomes
chromosome 14q
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Downregulation of ZC3H14 driven by chromosome 14q31 deletion promotes hepatocellular carcinoma progression by activating integrin signaling.
Chuxiao Zhang
,
Pengbo Cao
,
+7 authors
Gangqiao Zhou
Carcinogenesis
2018
Corpus ID: 53105551
Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related mortality worldwide. Genomic copy number deletion at…
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2009
2009
Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations.
C. Chen
,
S. Chern
,
E. Tsai
,
C. Lee
,
L. F. Chen
,
W. Wang
Genetic Counseling
2009
Corpus ID: 6983756
The fetus was the 1096-g product of 28-week gestation in a 31-yearold, gravida 2, para 1, mother who had undergone amniocentesis…
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2007
2007
An innocuous duplication of 11.2 Mb at 13q21 is gene poor: Sub‐bands of gene paucity and pervasive CNV characterize the chromosome anomalies
A. Daniel
,
A. Darmanian
,
G. Peters
,
L. Goodwin
,
Jason R. Hort
American Journal of Medical Genetics. Part A
2007
Corpus ID: 35513499
A boy with autistic spectrum disorder without dysmorphisms was found to have a chromosome duplication of part of band 13q21. His…
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2006
2006
Identification of a 7.1-mega base pairs minimal deletion at 14q31.1-32.11 in adenocarcinomas of the gastroesophageal junction.
W. Dinjens
,
L. Koppert
,
+6 authors
B. Wijnhoven
Human Pathology
2006
Corpus ID: 20535043
2000
2000
Multiple cranial nerve enhancement in early infantile Krabbe’s disease
Oscar Bernal
,
N. Lenn
Neurology
2000
Corpus ID: 7530912
Krabbe’s disease or globoid-cell leukodystrophy is an autosomal recessive disorder caused by a mutation of the galactocerebroside…
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1999
1999
Gene structure, chromosomal location, and expression pattern of maleylacetoacetate isomerase.
J. Fernández-Cañón
,
Jim Hejna
,
C. Reifsteck
,
Susan B. Olson
,
Markus Grompe
Genomics
1999
Corpus ID: 24006271
The gene for maleylacetoacetate isomerase (MAAI) (EC 5.2.1.2) was the last gene in the mammalian phenylalanine/tyrosine catabolic…
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