pubmed-article:7990924 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7990924 | lifeskim:mentions | umls-concept:C1522384 | lld:lifeskim |
pubmed-article:7990924 | lifeskim:mentions | umls-concept:C0596142 | lld:lifeskim |
pubmed-article:7990924 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
pubmed-article:7990924 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:7990924 | lifeskim:mentions | umls-concept:C1861922 | lld:lifeskim |
pubmed-article:7990924 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
pubmed-article:7990924 | pubmed:issue | 6506 | lld:pubmed |
pubmed-article:7990924 | pubmed:dateCreated | 1995-1-10 | lld:pubmed |
pubmed-article:7990924 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7990924 | pubmed:abstractText | Induction of testis development in mammals requires the presence of the Y-chromosome gene SRY. This gene must exert its effect by interacting with other genes in the sex-determination pathway. Cloning of a translocation chromosome breakpoint from a sex-reversed patient with campomelic dysplasia, followed by mutation analysis of an adjacent gene, indicates that SOX9, an SRY-related gene, is involved in both bone formation and control of testis development. | lld:pubmed |
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pubmed-article:7990924 | pubmed:language | eng | lld:pubmed |
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pubmed-article:7990924 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:7990924 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7990924 | pubmed:month | Dec | lld:pubmed |
pubmed-article:7990924 | pubmed:issn | 0028-0836 | lld:pubmed |
pubmed-article:7990924 | pubmed:author | pubmed-author:GoodfellowP... | lld:pubmed |
pubmed-article:7990924 | pubmed:author | pubmed-author:WeissenbachJJ | lld:pubmed |
pubmed-article:7990924 | pubmed:author | pubmed-author:YoungI DID | lld:pubmed |
pubmed-article:7990924 | pubmed:author | pubmed-author:MansourSS | lld:pubmed |
pubmed-article:7990924 | pubmed:author | pubmed-author:FosterJ WJW | lld:pubmed |
pubmed-article:7990924 | pubmed:author | pubmed-author:Stevanovi?MM | lld:pubmed |
pubmed-article:7990924 | pubmed:author | pubmed-author:GuioliSS | lld:pubmed |
pubmed-article:7990924 | pubmed:author | pubmed-author:WellerP APA | lld:pubmed |
pubmed-article:7990924 | pubmed:author | pubmed-author:KwokCC | lld:pubmed |
pubmed-article:7990924 | pubmed:author | pubmed-author:Dominguez-Ste... | lld:pubmed |
pubmed-article:7990924 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7990924 | pubmed:day | 8 | lld:pubmed |
pubmed-article:7990924 | pubmed:volume | 372 | lld:pubmed |
pubmed-article:7990924 | pubmed:geneSymbol | SOX9 | lld:pubmed |
pubmed-article:7990924 | pubmed:geneSymbol | SRY | lld:pubmed |
pubmed-article:7990924 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7990924 | pubmed:authorsComplete | N | lld:pubmed |
pubmed-article:7990924 | pubmed:pagination | 525-30 | lld:pubmed |
pubmed-article:7990924 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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pubmed-article:7990924 | pubmed:year | 1994 | lld:pubmed |
pubmed-article:7990924 | pubmed:articleTitle | Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene. | lld:pubmed |
pubmed-article:7990924 | pubmed:affiliation | Department of Genetics, University of Cambridge, UK. | lld:pubmed |
pubmed-article:7990924 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:7990924 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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