1 Alter BP, Baerlocher GM, Savage SA et al. Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita. Blood 2007; 110: 1439–47. 2 Walne… Click to show full abstract
1 Alter BP, Baerlocher GM, Savage SA et al. Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita. Blood 2007; 110: 1439–47. 2 Walne AJ, Dokal I. Advances in the understanding of dyskeratosis congenita. Br. J. Haematol. 2009; 145: 164–72. 3 Yabe M, Yabe H, Hattori K et al. Fatal interstitial pulmonary disease in a patient with dyskeratosis congenita after allogeneic bone marrow transplantation. Bone Marrow Transplant. 1997; 19: 389–92. 4 Tummala H, Walne A, Collopy L et al. Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita. J. Clin. Invest. 2015; 125: 2151–60. 5 Walne AJ, Vulliamy T, Beswick R et al. TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes. Blood 2008; 112: 3594–600.
               
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