The clinical impact of copy number variants in inherited bone marrow failure syndromes - Waespe, Nicolas; Dhanraj, Santhosh; Wahala, Manju; Tsangaris, Elena; Enbar, Tom; Zlateska, Bozana; Li, Hongbing; Klaassen, Robert J.; Fernandez, Conrad V.; Cuvelier, Geoff D. E.; Wu, John K.; Pastore, Yves D.; et al. (Npj genomic medicine, 2017)
Keywords: 631/1647/2163; 631/1647/2217/2136; 631/208/2489/1512; 631/208/727/2000; 631/67/2332; Bioinformatics; Biomedical and Life Sciences; Biomedicine; Bone marrow; Gene Function; Gene Therapy; Human Genetics; Internal Medicine; Mutation; Biological sciences/Cancer/Paediatric cancer; Biological sciences/Genetics/Clinical genetics/Genetic testing; Biological sciences/Biological techniques/High-throughput screening; Biological sciences/Biological techniques/Genomic analysis/Comparative genomic hybridization; Biological sciences/Genetics/Genotype/Genetic predisposition to disease