H. Schneider

Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia.

Kenneth Offit, Mark Robson, Larry Norton, 2003, Journal of the National Cancer Institute.

Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype.

G. Pals, J. Soulier, J. Surrallés, 2007, American journal of human genetics.

Correct mRNA processing at a mutant TT splice donor in FANCC ameliorates the clinical phenotype in patients and is enhanced by delivery of suppressor U1 snRNAs.

S. Burdach, D. Schindler, A. Auerbach, 2010, American journal of human genetics.

Spectrum of sequence variation in the FANCG gene: An International Fanconi Anemia Registry (IFAR) study

J. Greenbaum, P. Giampietro, S. Batish, 2003 .

Spectrum of sequence variation in the FANCG gene: An International Fanconi Anemia Registry (IFAR) study

J. Greenbaum, P. Giampietro, S. Batish, 2003, Human mutation.