Hypomorphic Mutations in the Central Fanconi Anemia Gene FANCD2 Sustain a Significant Group of FA-D2 Patients with Severe Phenotype.

R. Kalb, K. Neveling, H. Hoehn, K. Goettsche, S.D. Battish, C. Hunt, M. Berwick, E. Callén, J. Surrallés, J.A. Casado, J.A. Bueren, A. Dasí, C.M. Zwaan, R. Vervenne, Pals

Research output: Contribution to journalArticleResearch

86 Citations (Scopus)
Original languageEnglish
Pages (from-to)895-910
JournalAmerican Journal of Human Genetics
Volume80
Publication statusPublished - 1 Jan 2007

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