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Xp22.32

A chromosome band present on Xp
National Institutes of Health

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6 relations
CD99 wt AlleleCSF2RA wt AlleleChromosomesKAL1 wt Allele

Papers overview

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2017
2017
Lack of decussation of pyramids in Kallmann syndrome presenting with mirror movements
2012
2012
[Molecular and cytogenetic characterization of six 46, XX males due to translocations between the short arms of X and Y chromosomes].
  • Y. XingX. Ji J. Tao
  • Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
  • 2012
  • Corpus ID: 24646577
OBJECTIVE To characterize molecular and cytogenetic abnormalities in six 46, XX males, and to investigate the clinical… 
2011
2011
Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1
Ebstein anomaly is an uncommon congenital heart defect (CHD), characterized by downward displacement of the tricuspid valve into… 
2009
2009
Identification of a novel human endogenous retrovirus and promoter activity of its 5' U3.
Review
2002
Review
2002
New insights into ocular albinism type 1 (OA1): Mutations and polymorphisms of the OA1 gene
Albinism ocular type 1 (OA1) is an X‐linked type of albinism that mainly effects pigment production in the eye, resulting in… 
2002
2002
Detection of microdeletions in the short arm of the X chromosome by chromosome stretching
The present study was focused on the resolution of “chromosome stretching”. In order to determine if this method can be used for… 
1996
1996
Short stature in a mother and daughter with terminal deletion of Xp22.3.
Short stature in females is often caused by hemizygosity for the terminal portion of Xp due to monosomy X or a deletion. We… 
1993
1993
Deletion analysis maps ocular albinism proximal to the steroid sulphatase locus
We describe a pedigree in which four male members are affected by a contiguous gene abnormality involving the short arm of the X… 
Review
1991
Review
1991
Pericentric inversion of the X chromosome: presentation of a case and review of the literature.
A large pericentric inversion of the X chromosome [inv(X)(p22.31q26.3)] was found to be transmitted in four generations through… 
Review
1985
Review
1985
Homologous expressed genes in the human sex chromosome pairing region
The human sex chromosomes share a pair of homologous genes which independently encode a cell-surface antigen defined by the… 
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