rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
2
|
pubmed:dateCreated |
2008-2-4
|
pubmed:abstractText |
Adolescent idiopathic scoliosis (AIS) is the most common form of spinal deformity, affecting up to 4% of children worldwide. Familial inheritance of AIS is now recognised and several potential candidate loci have been found.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
1468-6244
|
pubmed:author |
pubmed-author:BriceGG,
pubmed-author:ChildA HAH,
pubmed-author:EbenezerN DND,
pubmed-author:HardcastleA JAJ,
pubmed-author:MehtaMM,
pubmed-author:MorleyTT,
pubmed-author:O'DowdJJ,
pubmed-author:OcakaLL,
pubmed-author:ReedJ AJA,
pubmed-author:WeberJ LJL,
pubmed-author:ZhaoCC
|
pubmed:issnType |
Electronic
|
pubmed:volume |
45
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
87-92
|
pubmed:meshHeading |
pubmed-meshheading:17932119-Adolescent,
pubmed-meshheading:17932119-Chromosome Mapping,
pubmed-meshheading:17932119-Chromosomes, Human, Pair 17,
pubmed-meshheading:17932119-Chromosomes, Human, Pair 9,
pubmed-meshheading:17932119-Female,
pubmed-meshheading:17932119-Genes, Dominant,
pubmed-meshheading:17932119-Genotype,
pubmed-meshheading:17932119-Humans,
pubmed-meshheading:17932119-Lod Score,
pubmed-meshheading:17932119-Male,
pubmed-meshheading:17932119-Phenotype,
pubmed-meshheading:17932119-Scoliosis
|
pubmed:year |
2008
|
pubmed:articleTitle |
Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.
|
pubmed:affiliation |
Department of Cardiological Sciences, St George's Medical School, University of London, UK.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|