A second locus for Rieger syndrome maps to chromosome 13q14.

Rieger syndrome is a genetically and phenotypically heterogeneous disorder typically characterized by malformations of the eyes, teeth, and umbilicus. The syndrome is inherited as an autosomal dominant trait and exhibits significant variable expressivity. One locus associated with this disorder has...

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Bibliografiset tiedot
Päätekijät: Phillips, J. C., del Bono, E. A., Haines, J. L., Pralea, A. M., Cohen, J. S., Greff, L. J., Wiggs, J. L.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1996
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Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1914897/
https://ncbi.nlm.nih.gov/pubmed/8751862
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