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The New England Journal of Medicine, ISSN 0028-4793, 12/2015, Volume 373, Issue 24, pp. 2336 - 2346
Journal Article
Journal Article
HAEMATOLOGICA, ISSN 0390-6078, 09/2019, Volume 104, Issue 10, pp. 1962 - 1973
Fanconi anemia is a rare recessive disease characterized by multiple congenital abnormalities, progressive bone marrow failure, and a predisposition to... 
GENE | VARIANTS | X-LINKED VACTERL | BILATERAL BREAST-CANCER | GERMLINE MUTATIONS | CONSEQUENCES | HOMOLOGOUS RECOMBINATION | BIALLELIC MUTATIONS | BRCA2 | HEMATOLOGY | BONE-MARROW FAILURE
Journal Article
Cancer Research, ISSN 0008-5472, 10/2010, Volume 70, Issue 19, pp. 7353 - 7359
Journal Article
PLOS GENETICS, ISSN 1553-7404, 03/2016, Volume 12, Issue 3
Patients with biallelic truncating mutations in PALB2 have a severe form of Fanconi anaemia (FA-N), with a predisposition for developing embryonal-type tumours... 
BREAST-CANCER | CELLS | REPAIR | GENETICS & HEREDITY | GERMLINE MUTATIONS | SHARED GENETIC SUSCEPTIBILITY | OVARIAN-CANCER | HOMOLOGOUS RECOMBINATION | BIALLELIC MUTATIONS | BRCA2 | FANCONI-ANEMIA SUBTYPE
Journal Article
Expert Review of Anticancer Therapy, ISSN 1473-7140, 09/2019, Volume 19, Issue 9, pp. 787 - 801
Journal Article
Journal Article