|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0008667,
umls-concept:C0017337,
umls-concept:C0023745,
umls-concept:C0205369,
umls-concept:C0271097,
umls-concept:C0332120,
umls-concept:C0332307,
umls-concept:C0449432,
umls-concept:C1179435,
umls-concept:C1257890,
umls-concept:C1524073,
umls-concept:C1548799,
umls-concept:C1705248
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|
pubmed:issue |
2
|
|
pubmed:dateCreated |
1990-12-5
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|
pubmed:abstractText |
A linkage of the gene for Usher's syndrome with group specific component (GC) on the long arm of chromosome 4 has been suggested by Pelias et al., in 1988. A panel of 38 individuals from 7 kindreds with Usher's syndrome type 1 has been established to test this hypothesis. A negative lodscore was found and close linkage was excluded.
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|
pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:issn |
0003-3995
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
33
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
103-4
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|
pubmed:dateRevised |
2004-11-17
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|
pubmed:meshHeading |
pubmed-meshheading:2241083-Abnormalities, Multiple,
pubmed-meshheading:2241083-Child,
pubmed-meshheading:2241083-Chromosomes, Human, Pair 4,
pubmed-meshheading:2241083-Female,
pubmed-meshheading:2241083-Genes, Recessive,
pubmed-meshheading:2241083-Hearing Loss, Bilateral,
pubmed-meshheading:2241083-Hearing Loss, Sensorineural,
pubmed-meshheading:2241083-Humans,
pubmed-meshheading:2241083-Lod Score,
pubmed-meshheading:2241083-Male,
pubmed-meshheading:2241083-Retinitis Pigmentosa,
pubmed-meshheading:2241083-Syndrome,
pubmed-meshheading:2241083-Vitamin D-Binding Protein
|
|
pubmed:year |
1990
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|
pubmed:articleTitle |
Evidence against linkage of the gene for Usher's syndrome type 1 with group specific component (GC) on chromosome 4.
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|
pubmed:affiliation |
Service de Pédiatrie, Centre Hospitalier Régional Universitaire de Poitiers, France.
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pubmed:publicationType |
Journal Article
|
