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6q25.3
A chromosome band present on 6q
National Institutes of Health
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4 relations
Chromosomes
GTF2H5 wt Allele
SLC22A1 wt Allele
SOD2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2020
Review
2020
Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion.
Giulia Pascolini
,
M. Valiante
,
+4 authors
P. Grammatico
European Journal of Medical Genetics
2020
Corpus ID: 201057894
2020
2020
A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short‐lived infant
M. G. Domínguez
,
H. Rivera
,
Rosa María Dávalos-Pulido
,
I. Dávalos-Rodríguez
Journal of clinical laboratory analysis (Print)
2020
Corpus ID: 218617848
Non‐acrocentric satellited chromosomes mostly result from familial balanced insertions or translocations with p12 or p13 of any…
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2015
2015
Congenital hydrocephalus and hemivertebrae associated with de novo partial monosomy 6q (6q25.3→qter)
Y. Li
,
K. Choy
,
+8 authors
X.-J. Chen
Balkan Journal of Medical Genetics
2015
Corpus ID: 13599227
Abstract This study was conducted to describe a prenatal case of congenital hydrocephalus and hemivertebrae with a 6q terminal…
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2011
2011
Medulloblastoma: Origins
N. McCarthy
Nature Reviews. Cancer
2011
Corpus ID: 1688449
a range of distinct brain tumour subtypes that arise in childhood and have long been associated with the cerebellum. However…
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2009
2009
Characterization of a complex chromosome aberration in two cases of peritoneal mesothelioma arising primarily in the hernial sac
G. Serio
,
M. Gentile
,
+6 authors
A. Scattone
Pathology international (Print)
2009
Corpus ID: 44305041
Malignant mesotheliomas of the hernial sac are uncommon and only a few cases have been diagnosed incidentally during…
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2006
2006
A locus for sacral/anorectal malformations maps to 6q25.3 in a 0.3 Mb interval region
L. Titomanlio
,
I. Giurgea
,
+5 authors
A. Verloes
European Journal of Human Genetics
2006
Corpus ID: 24553725
Partial absence of the sacrum is a rare congenital defect that also occurs as an autosomal-dominant trait, whereas imperforate…
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2002
2002
[Genescan analysis of non-small cell lung cancer in the long arm of chromosome 6].
Huiying Gao
,
Qi Wang
,
+6 authors
S. Fu
Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
2002
Corpus ID: 24369194
OBJECTIVE To investigate if there are microsatellite loci in the long arm of chromosome 6 that have close relationship with non…
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Review
2001
Review
2001
Terminal 6q25.3 deletion and abnormal behaviour.
T. Lukusa
,
D. Willekens
,
N. Lukusa
,
F. de Cock
,
J. Fryns
Genetic Counseling
2001
Corpus ID: 10044981
A 10-year-old mentally retarded boy with terminal 6q25 deletion, dysmorphism and striking abnormal behaviour is reported. The…
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2000
2000
Mapping of Target Regions of Allelic Loss in Primary Breast Cancers to 1‐cM Intervals on Genomic Contigs at 6q21 and 6q25.3
Y. Utada
,
S. Haga
,
+4 authors
M. Emi
Japanese journal of cancer research : Gann
2000
Corpus ID: 13708486
Allelic losses on the long arm of human chromosome 6 are frequently observed in cancers of the ovary, prostate, and breast. To…
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1999
1999
Syndromal obesity due to paternal duplication 6(q24.3-q27).
A. Smith
,
A. Jauch
,
H. Slater
,
L. Robson
,
T. Sandanam
American journal of medical genetics
1999
Corpus ID: 23663795
The likelihood of a paternally expressing imprinted gene in chromosome region 6(q23-24) has been highlighted by cases of…
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