Xp22.3

A chromosome band present on Xp
National Institutes of Health

Papers overview

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2007
2007
Turner syndrome (TS) is associated with a neurocognitive phenotype that includes selective nonverbal deficits, e.g., impaired… (More)
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Highly Cited
2005
Highly Cited
2005
SIR—Jamain et al reported a frameshift and a mis sense mutation in the X-linked neuroligin 4 (NLGN4, MIM# 300427) and neuroligin… (More)
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2000
2000
X-linked nonspecific mental retardation (MRX) has a frequency of 0.15% in the male population and is caused by defects in several… (More)
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2000
2000
We describe monozygotic male twins with an interstitial deletion of Xp22.3 including the steroid sulphatase gene (STS). The twins… (More)
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1998
1998
It has been proposed that the pseudoautosomal region of mammals has evolved by sequential addition of autosomal material onto the… (More)
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Highly Cited
1995
Highly Cited
1995
X-linked recessive chondrodysplasia punctata (CDPX) is a congenital defect of bone and cartilage development characterized by… (More)
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1995
1995
We have isolated a gene, PKX1, by virtue of its position within the candidate region for chondrodysplasia punctata in Xp22.3… (More)
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1994
1994
In the framework of constructing a comprehensive transcript map of the human Xp22.3 region, we identified an evolutionary… (More)
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1992
1992
Patients with Kallmann's syndrome show hypothalamic hypogonadism, hyposmia, and congenital mirror movements. As a correlate, a… (More)
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1990
1990
We describe two females with de novo X;Y translocations, who presented at birth with irregular linear areas of erythematous skin… (More)
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