Gene List:
ACD, AK2, ANKRD26, AP3B1, ATM, BLM, BRCA1, BRCA2, BRIP1, CBL, CEBPA, CSF3R, CTC1, CXCR4, DDX41, DKC1, DNAJC21, ELANE, EPCAM, ERCC4, ETV6, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, G6PC3, GATA1, GATA2, GFI1, HAX1, IKZF1, LAMTOR2, LYST, MLH1, MPL, MSH2, MSH6, NBN, NF1, NHP2, NOP10, PALB2, PAX5, PMS2, PTPN11, RAB27A, RAC2, RAD51C, RBM8A, RMRP, RPL11, RPL15, RPL26, RPL35A, RPL5, RPS10, RPS17, RPS19, RPS24, RPS26, RPS28, RPS29, RPS7, RTEL1, RUNX1, SAMD9, SAMD9L, SBDS, SLC37A4, SLX4, SRP72, TAZ, TERC, TERT, TINF2, TP53, UBE2T, USB1, VPS13B, VPS45, WAS, WRAP53, XRCC2

References:
Mehta PA, Tolar J. Fanconi Anemia. Gene Reviews. Pagon RA, Adam MP, Ardinger HH, et al., editors. Seattle (WA): University of Washington, Seattle; 1993-2016.

Dokal I, Vulliamy T, Mason P, Bessler M. Clinical utility gene card for: Dyskeratosis congenita–update 2015. European Journal of Human Genetics. 2015 Apr;23(4).

Alter BP, Giri N, Savage SA, Peters JA, Loud JT, Leathwood L, Carr AG, Greene MH, Rosenberg PS. Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study. British journal of haematology. 2010 Jul;150(2):179-88.