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Radiation Research|February 26, 2004
Lack of sensitivity of primary Fanconi's anemia fibroblasts to UV and ionizing radiationReinhard Kalb, Michael Duerr, Matthias Wagner, et al.European Journal of Pediatrics|January 18, 2006
Exclusion/confirmation of ataxia-telangiectasia via cell-cycle testingTilman Heinrich, Carolin Prowald, Richard Friedl, et al.Fetal Diagnosis and Therapy|December 16, 2005
Prenatal exclusion/confirmation of Fanconi anemia via flow cytometry: a pilot studyAstrid Bechtold, Richard Friedl, Reinhard Kalb, et al.International Journal of Molecular Sciences|July 29, 2025
<i>BRCA2</i> Pre-mRNA Differential 5' Splicing: A Rescue of Functional Protein Properties from Pathogenic Gene Variants and a Lifeline for Fanconi Anemia D1 PatientsRoberto Paredes, Kiran Batta, Daniel H Wiseman, et al.The Journal of Clinical Investigation|April 15, 2025
Genetic inactivation of FAAP100 causes Fanconi anemia due to disruption of the monoubiquitin ligase core complexJulia Kuehl, Yutong Xue, Fenghua Yuan, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 1, 2021
Cancer in Children With Fanconi Anemia and Ataxia-Telangiectasia-A Nationwide Register-Based Cohort Study in GermanyChristina M Dutzmann, Claudia Spix, Isabell Popp, et al.British Journal of Haematology|April 14, 2006
Delayed diagnosis and complications of Fanconi anaemia at advanced age--a paradigmKirsten Huck, Helmut Hanenberg, Sonja Gudowius, et al.Plos One|August 10, 2011
Fanconi anemia core complex gene promoters harbor conserved transcription regulatory elementsDaniel Meier, Detlev SchindlerThe EMBO Journal|February 17, 2007
Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stabilityMassimo Bogliolo, Alex Lyakhovich, Elsa Callén, et al.American Journal of Human Genetics|May 5, 2009
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorderRegina Waltes, Reinhard Kalb, Magtouf Gatei, et al.Pageof 13