|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
1
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|
pubmed:dateCreated |
2001-10-11
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|
pubmed:abstractText |
To identify possible mutations in our previously cloned candidate gene for hereditary multiple exostoses type II (EXT2) in affected members of EXT families so as to confirm that it is the disease-causing gene.
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pubmed:language |
eng
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|
pubmed:journal |
|
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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|
pubmed:issn |
0366-6999
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
112
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
72-5
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|
pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11593646-Amino Acid Sequence,
pubmed-meshheading:11593646-Base Sequence,
pubmed-meshheading:11593646-Bone Neoplasms,
pubmed-meshheading:11593646-Chondrosarcoma,
pubmed-meshheading:11593646-Chromosomes, Human, Pair 11,
pubmed-meshheading:11593646-Chromosomes, Human, Pair 8,
pubmed-meshheading:11593646-DNA, Neoplasm,
pubmed-meshheading:11593646-Exostoses, Multiple Hereditary,
pubmed-meshheading:11593646-Humans,
pubmed-meshheading:11593646-Loss of Heterozygosity,
pubmed-meshheading:11593646-Molecular Sequence Data,
pubmed-meshheading:11593646-Point Mutation
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|
pubmed:year |
1999
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|
pubmed:articleTitle |
Identification of mutation in a candidate gene for hereditary multiple exostoses type II.
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|
pubmed:affiliation |
National Laboratory of Medical Genetics, Hunan Medical University, Changsha 410078, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
