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Frequent Chromosome Aberrations Revealed by Molecular Cytogenetic Studies in Patients with Aniridia
Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilms tumor risk, were studied by fluorescence in situ hybridization (FISH), through use of a panel of cosmids encompassing the aniridia-associated PAX6 gene, the Wilms tumor predisposition gene WT1, and...
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| Publicado no: | Am J Hum Genet |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2002
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC385089/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12386836/ https://ncbi.nlm.nih.govhttps://doi.org/10.1086/344396 |
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