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Genetic Basis of Prune Belly Syndrome: Screening for HNF1β Gene
PURPOSE: Although the cause of prune belly syndrome is unknown, familial evidence suggests a genetic component. Recently 2 nonfamilial cases of prune belly syndrome with chromosome 17q12 deletions encompassing the HNF1β gene have made this a candidate gene for prune belly syndrome. To date, there ha...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3399512/ https://ncbi.nlm.nih.gov/pubmed/22114815 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.juro.2011.09.036 |
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