Source:http://linkedlifedata.com/resource/pubmed/id/10025779
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1999-4-23
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pubmed:abstractText |
1) To confirm linkage of hereditary sensory neuropathy type 1 (HSN-I) to human chromosome 9q22 in a large American family of German origin. 2) To construct a yeast artificial chromosome (YAC) contig spanning the HSN-I candidate interval. 3) To investigate the HSN-I contig for potential candidate genes.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0028-3878
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
52
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
510-5
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:10025779-Chromosome Mapping,
pubmed-meshheading:10025779-Chromosomes, Human, Pair 9,
pubmed-meshheading:10025779-Female,
pubmed-meshheading:10025779-Genetic Linkage,
pubmed-meshheading:10025779-Haplotypes,
pubmed-meshheading:10025779-Hereditary Sensory and Autonomic Neuropathies,
pubmed-meshheading:10025779-Humans,
pubmed-meshheading:10025779-Male,
pubmed-meshheading:10025779-Pedigree
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pubmed:year |
1999
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pubmed:articleTitle |
Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22.
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pubmed:affiliation |
Day Neuromuscular Research Laboratory, Massachusetts General Hospital, Boston, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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