Chromosome 6, monosomy 6q

Known as: Deletion 6q, Monosomy 6q 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1987-2015
01219872015

Papers overview

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2015
2015
This study was conducted to describe a prenatal case of congenital hydrocephalus and hemivertebrae with a 6q terminal deletion… (More)
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2009
2009
OBJECTIVE We investigated the application of microarray-based comparative genomic hybridization (array CGH) on a fetus showing… (More)
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2003
2003
Here we describe a foetus with intrauterine growth retardation (IUGR), cerebral malformations and a 46,XY,der(1),t(1;6)(p36.3;q25… (More)
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2003
2003
6q-syndrome is a rare disorder characterised by a combination of anatomic anomalies, and mental and motor retardation due to a… (More)
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1996
1996
A cytogenetic discrepancy in chorionic villi with implications for prenatal diagnosis is described. Chromosome analysis revealed… (More)
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Review
1996
Review
1996
Two children with a partial monosomy 6q are reported: a girl with an interstitial deletion [46,XX,del(6)(q16.2q23.1)], and a boy… (More)
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1993
1993
We report the prenatal diagnosis of a karyotype 46,XY,rec(6)dup p, inv(6) (p23q27) mat detected by fluorescence in situ… (More)
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1987
1987
We report a child, now aged two years, who is monosomic for the region 6q23.1----q24.2. Her mother, older sister, and twin sister… (More)
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