Loading...
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...
Na minha lista:
| Udgivet i: | Am J Hum Genet |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Elsevier
2002
|
| Fag: | |
| Online adgang: | 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 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|