| pubmed-article:11551104 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11551104 | lifeskim:mentions | umls-concept:C0015176 | lld:lifeskim |
| pubmed-article:11551104 | lifeskim:mentions | umls-concept:C0920317 | lld:lifeskim |
| pubmed-article:11551104 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:11551104 | lifeskim:mentions | umls-concept:C1415077 | lld:lifeskim |
| pubmed-article:11551104 | lifeskim:mentions | umls-concept:C0439603 | lld:lifeskim |
| pubmed-article:11551104 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:11551104 | pubmed:dateCreated | 2001-9-11 | lld:pubmed |
| pubmed-article:11551104 | pubmed:abstractText | Mutations in the gene encoding connexin-26 (specified GJB2) have been shown to be a major cause of nonsyndromic recessive deafness (NSRD), and a single mutation 35delG in the GJB2 gene accounts for the majority of cases of NSRD. This mutation was screened in France and in other European populations by a reliable PCR method. We present here a meta-analysis of the 35delG frequencies in 4123 random controls from 20 European countries, and show that the mutation is more frequent in the south of Europe than in the north; a north-south increasing cline of 35delG frequencies is established (r = -0.527). | lld:pubmed |
| pubmed-article:11551104 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11551104 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11551104 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:11551104 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11551104 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11551104 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11551104 | pubmed:issn | 1090-6576 | lld:pubmed |
| pubmed-article:11551104 | pubmed:author | pubmed-author:LucotteGG | lld:pubmed |
| pubmed-article:11551104 | pubmed:author | pubmed-author:MercierGG | lld:pubmed |
| pubmed-article:11551104 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11551104 | pubmed:volume | 5 | lld:pubmed |
| pubmed-article:11551104 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11551104 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11551104 | pubmed:pagination | 149-52 | lld:pubmed |
| pubmed-article:11551104 | pubmed:dateRevised | 2006-3-28 | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:meshHeading | pubmed-meshheading:11551104... | lld:pubmed |
| pubmed-article:11551104 | pubmed:year | 2001 | lld:pubmed |
| pubmed-article:11551104 | pubmed:articleTitle | Meta-analysis of GJB2 mutation 35delG frequencies in Europe. | lld:pubmed |
| pubmed-article:11551104 | pubmed:affiliation | International Institute of Anthropology, Paris, France. lucotte@hotmail.com | lld:pubmed |
| pubmed-article:11551104 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11551104 | pubmed:publicationType | Meta-Analysis | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11551104 | lld:pubmed |
