Hypomorphic mutations in the gene encoding a key fanconi anemia protein, fancd2, sustain a significant group of fa-d2 patients with severe phenotype

R Kalb, K Neveling, H Hoehn, H Schneider, Y Linka, SD Batish, C Hunt, M Berwick, E Callen, J Surralles, JA Casado, J Bueren, A Dasi, J Soulier, E Gluckman, C.M. Zwaan, RML (Rosalina) van Spaendonk, G Pals, JP (Johan) de Winter, H JoenjeM Grompe, AD Auerbach, H Hanenberg, D Schindler

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)895-910
Number of pages16
JournalAmerican Journal of Human Genetics
Volume80
DOIs
Publication statusPublished - 2007

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