Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome

The Langer-Giedion syndrome (LGS), which is characterized by craniofacial dysmorphism and skeletal abnormalities, is caused by a genetic defect in 8q24.1. We have used 13 anonymous DNA markers from an 8q24.1-specific microdissection library, as well as c-myc and thyroglobulin gene probes, to map the...

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Main Authors: Lüdecke, Hermann-Josef, Johnson, Carey, Wagner, Michael J., Wells, Dan E., Turleau, Catherine, Tommerup, Niels, Latos-Bielenska, Anna, Sandig, Klaus-Rainer, Meinecke, Peter, Zabel, Bernhard, Horsthemke, Bernhard
Formato: Artigo
Idioma:Inglês
Publicado em: 1991
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1686450/
https://ncbi.nlm.nih.gov/pubmed/1836105
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