Xp22.32

A chromosome band present on Xp
National Institutes of Health

Topic mentions per year

Topic mentions per year

1985-2011
01219852011

Papers overview

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2012
2012
OBJECTIVE To characterize molecular and cytogenetic abnormalities in six 46, XX males, and to investigate the clinical… (More)
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2011
2011
Ebstein anomaly is an uncommon congenital heart defect (CHD), characterized by downward displacement of the tricuspid valve into… (More)
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2009
2009
Up-regulation of human endogenous retroviruses (HERVs) sometimes occurs in cancer. This study identifies a novel HERV (HERV-HX… (More)
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2008
2008
BACKGROUND X-linked ichthyosis (XLI) (steroid sulfatase deficiency) is caused by deletions or point mutations of the steroid… (More)
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2001
2001
BACKGROUND/AIMS Leri-Weill dyschondrosteosis (LWD), a mesomelic short stature syndrome with Madelung deformity, was recently… (More)
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2001
2001
The present study was focused on the resolution of "chromosome stretching". In order to determine if this method can be used for… (More)
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1996
1996
Short stature in females is often caused by hemizygosity for the terminal portion of Xp due to monosomy X or a deletion. We… (More)
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1993
1993
We describe a pedigree in which four male members are affected by a contiguous gene abnormality involving the short arm of the X… (More)
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Review
1991
Review
1991
A large pericentric inversion of the X chromosome [inv(X)(p22.31q26.3)] was found to be transmitted in four generations through… (More)
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Review
1985
Review
1985
The human sex chromosomes share a pair of homologous genes which independently encode a cell-surface antigen defined by the… (More)
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