Author:
Hipp Lauren E.,Milliron Kara J.,Hulswit Bailey B.,Merajver Sofia D.
Reference75 articles.
1. Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2;Alter;J. Med. Genet.,2007
2. Ambry Genetics, (2018). Breaking new ground through high-quality genetic testing. Nature Portfolio.
3. Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases;Anglian Breast Cancer Study Group;Br. J. Cancer,2000
4. Antonarakis, S. and Hamosh, A. (2001). Fanconi anemia, complementation group D1
5. FANCD1, 2001. Available online: https://omim.org/entry/605724?search=fancd1&highlight=fancd1.