Xp22

A chromosome band present on Xp
National Institutes of Health

Topic mentions per year

Topic mentions per year

1978-2017
051019782017

Papers overview

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2008
2008
The evaluation of four pairs of tightly linked chromosome X (ChrX) short tandem repeat (STR)s at Xp22, Xq12, Xq26 and Xq28 led to… (More)
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1999
1999
We have identified a novel gene with homologies to the Drosophila Sex comb on midleg (Scm) gene from the short arm of the X… (More)
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1999
1999
We have identified a novel human gene during studies of a 1.3-Mb region of Xp22 between DXS418 and DXS999. A PAC contig spanning… (More)
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1998
1998
Eukaryotic protein kinases are part of a large and expanding family of proteins. Through our transcriptional mapping effort in… (More)
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1998
1998
Using exon trapping, we have identified a new human gene in Xp22 encoding a 3-kb mRNA. Expression of this RNA is detectable in a… (More)
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1998
1998
Microphthalmia with linear skin defects (MLS) is an X-linked dominant male-lethal syndrome caused by different deletions of… (More)
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1996
1996
Colony stimulating factor-2 receptor alpha (CSF2RA) and interleukin-3 receptor alpha (IL3RA), two genes from the chromosome Xp… (More)
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1994
1994
A gene responsible for a non-specific form of X-linked mental retardation (MRX19) was localised by linkage analysis. Exclusions… (More)
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1994
1994
We describe here a new type of X-linked liver glycogen storage disease. The main symptoms include liver enlargement and growth… (More)
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1993
1993
We have developed a 32–interval deletion panel for human chromosome Xp22 spanning about 30 megabases of genomic DNA. DNA samples… (More)
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