Unique phenotype associated with biallelic BRCA2 mutations includes high risk of brain tumors, Wilms tumors and early onset acute leukemia in children with Fanconi anemia Meeting Abstract
| Authors: | Auerbach, A. D.; Levran, O.; Mullaney, B.; Kutler, D. I.; Mah, K.; Deffenbaugh, A.; Scholl, T.; Berwick, M.; MacMillan, M. L.; Offit, K.; Wagner, J. E.; Hanenberg, H. |
| Abstract Title: | Unique phenotype associated with biallelic BRCA2 mutations includes high risk of brain tumors, Wilms tumors and early onset acute leukemia in children with Fanconi anemia |
| Meeting Title: | 53rd Annual Meeting of the American Society of Human Genetics (ASHG) |
| Journal Title: | American Journal of Human Genetics |
| Volume: | 73 |
| Issue: | 5 Suppl. |
| Meeting Dates: | 2003 Nov 4-8 |
| Meeting Location: | Los Angeles, CA |
| ISSN: | 0002-9297 |
| Publisher: | Cell Press |
| Date Published: | 2003-11-01 |
| Start Page: | 173 |
| Language: | English |
| ACCESSION: | WOS:000185599700056 |
| PROVIDER: | wos |
| PUBMED: | 14570018 |
| Notes: | Meeting Abstract: 55 -- Annual Meeting of the American-Society-of-Human-Genetics -- NOV 04-08, 2003 -- LOS ANGELES, CALIFORNIA -- Source: Wos |
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