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6p22.3
A chromosome band present on 6p
National Institutes of Health
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Related topics
Related topics
5 relations
Chromosome 6 Short Arm
Chromosomes
TPMT 3 Allele
TPMT*2 Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Association of CDKAL1 nucleotide variants with the risk of non-syndromic cleft lip with or without cleft palate
A. Gaczkowska
,
K. Żukowski
,
+8 authors
A. Mostowska
Journal of Human Genetics
2018
Corpus ID: 4365528
Although the aetiology of non-syndromic cleft lip with or without cleft palate (nsCL/P) has been studied extensively, knowledge…
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2017
2017
DEK protein level is a biomarker of CD138positive normal and malignant plasma cells
Zihni Onur Çalışkaner
,
Türkan Çakar
,
+7 authors
A. Kandilci
PLoS ONE
2017
Corpus ID: 26237451
Overexpression of DEK oncogene is associated with increased proliferation of carcinoma cells and it is observed in several solid…
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2011
2011
Variants on chromosome 6p22.3 associated with blood pressure in the HyperGEN study: follow-up of FBPP quantitative trait loci.
J. Simino
,
Gang Shi
,
D. Arnett
,
U. Broeckel
,
S. Hunt
,
D. Rao
American Journal of Hypertension
2011
Corpus ID: 15126112
BACKGROUND A recent meta-analysis of genome-wide linkage scans of blood pressure (BP) in the large (N = 13,044) Family Blood…
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2010
2010
Mild Intellectual Disability Associated with a Progeny of Father-Daughter Incest: Genetic and Environmental Considerations
F. Ansermet
,
J. Lespinasse
,
S. Gimelli
,
F. Béna
,
A. Paoloni-Giacobino
Journal of Child Sexual Abuse
2010
Corpus ID: 23800772
We report the case of a 34-year-old female resulting from a father-daughter sexual abuse and presenting a phenotype of mild…
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2009
2009
An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
A. Bremer
,
J. Schoumans
,
M. Nordenskjöld
,
B. Anderlid
,
M. Giacobini
European Journal of Medical Genetics
2009
Corpus ID: 6978673
2007
2007
E2F3 is responsible for frequent amplification of 6p22.3 in human bladder cancer
M. Oeggerli
2007
Corpus ID: 82319198
The 6p22 is generally regarded as one of the most important amplification sites in urinary bladder cancer. Investigations…
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2006
2006
The dysbindin gene (DTNBP1) and schizophrenia: No support for an association in the Korean population
E. Joo
,
K. Lee
,
S. Jeong
,
Y. Ahn
,
Y. Koo
,
Y. S. Kim
Neuroscience Letters
2006
Corpus ID: 29500714
2006
2006
Identification of chromosomal regions linked to premature myocardial infarction: a meta-analysis of whole-genome searches
E. Zintzaras
,
G. Kitsios
Journal of Human Genetics
2006
Corpus ID: 482147
AbstractMyocardial infarction (MI) is a complication of coronary artery disease and the leading cause of death in the Western…
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2006
2006
A genome‐wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba
B. Marcheco-Teruel
,
T. Flint
,
+9 authors
O. Mors
American Journal of Medical Genetics Part B…
2006
Corpus ID: 32472771
We present results from a genome‐wide scan of a six generation pedigree with 28 affected members with apparently dominant bipolar…
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Review
2003
Review
2003
Molecular genetics of schizophrenia: a review of the recent literature
D. Levinson
2003
Corpus ID: 18169765
Purpose of review The recent literature on the molecular genetics of schizophrenia is reviewed, to familiarize the reader with…
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