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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1994-7-18
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pubmed:abstractText |
Linkage data for familial incontinentia pigmenti (IP2) and 17 X chromosomal markers are reported. The linkage previously found between IP2 and the F8C locus is confirmed (Z max = 11.85 at theta = 0.028). Linkage is established with distal markers DXS1108 (Z max = 10.06 at theta = 0.00) and DXYS154 (Z = 9.07 at theta = 0.019). Multipoint analysis supports the distal localization of the IP2 gene with respect to the F8C locus.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
|
pubmed:issn |
0964-6906
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
3
|
pubmed:geneSymbol |
IP2,
Int22
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
N
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pubmed:pagination |
273-8
|
pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8004094-Animals,
pubmed-meshheading:8004094-Chromosome Mapping,
pubmed-meshheading:8004094-Eye Abnormalities,
pubmed-meshheading:8004094-Female,
pubmed-meshheading:8004094-Genes,
pubmed-meshheading:8004094-Genetic Markers,
pubmed-meshheading:8004094-Humans,
pubmed-meshheading:8004094-Incontinentia Pigmenti,
pubmed-meshheading:8004094-Lod Score,
pubmed-meshheading:8004094-Male,
pubmed-meshheading:8004094-Mice,
pubmed-meshheading:8004094-Pedigree,
pubmed-meshheading:8004094-Species Specificity,
pubmed-meshheading:8004094-X Chromosome
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pubmed:year |
1994
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pubmed:articleTitle |
The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28.
|
pubmed:affiliation |
Unité de Recherches sur les Handicaps Génétiquesde l'Enfant, INSERM U. 12, Hôpital Necker-Enfants Malades, Paris, France.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|