Dyskeratosis congenita in two male cousinsLOH, H. S; KOH, M. L; GIAM, Y. C et al.British journal of oral & maxillofacial surgery. 1987, Vol 25, Num 6, pp 492-499, issn 0266-4356Article

Dyskeratosis congenita associated with hypocellular myelodysplastic syndrome : A case reportENGIN, Hüseyin; KUZU, Isinsu; USTÜNDAG, Yücel et al.The American journal of the medical sciences. 2007, Vol 334, Num 3, pp 206-208, issn 0002-9629, 3 p.Article

Etiologic heterogeneity in dyskeratosis congenitaSHASHIDHAR PAI, G; MORGAN, S; WHETSELL, C et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 63-66, issn 0148-7299, 4 p.Article

Dyskeratosis congenita with pancytopeniaDODD, H. J; DEVEREUX, S; SARKANY, I et al.Clinical and experimental dermatology (Print). 1985, Vol 10, Num 1, pp 73-78, issn 0307-6938Article

Telomere dysfunction and tumor suppression responses in dyskeratosis congenita: Balancing cancer and tissue renewal impairmentHARTWIG, Fernando Pires; COLLARES, Tiago.Ageing research reviews. 2013, Vol 12, Num 2, pp 642-652, issn 1568-1637, 11 p.Article

Dyskeratosis congenita bei einem 40-jährigen Patienten = Dyskeratosis congenita in a 40-year-old patientBENOIT, S; KRAEMER, D; BRÖCKER, E.-B et al.Hautarzt. 2006, Vol 57, Num 4, pp 313-315, issn 0017-8470, 3 p.Article

Recent progress in dyskeratosis congenita : PIH: Recent advances in inherited bone marrow failure syndromesNISHIO, Nobuhiro; KOJIMA, Seiji.International journal of hematology. 2010, Vol 92, Num 3, pp 419-424, issn 0925-5710, 6 p.Article

Physiological assembly and activity of human telomerase complexesCOLLINS, Kathleen.Mechanisms of ageing and development. 2008, Vol 129, Num 1-2, pp 91-98, issn 0047-6374, 8 p.Article

Intensive immunosuppression therapy for aplastic anemia associated with dyskeratosis congenita : Report of a caseCOMOLI, Patrizia; BASSO, Sabrina; HUANG, Guan-Cheng et al.International journal of hematology. 2005, Vol 82, Num 1, pp 35-37, issn 0925-5710, 3 p.Article

Dyskeratosis congenita : A disorder of defective telomere maintenance?WALNE, Amanda J; MARRONE, Anna; DOKAL, Inderjeet et al.International journal of hematology. 2005, Vol 82, Num 3, pp 184-189, issn 0925-5710, 6 p.Article

Stem cell origin of the hematopoietic defect in dyskeratosis congenitaMARSH, J. C. W; WILL, A. J; HOWS, J. M et al.Blood. 1992, Vol 79, Num 12, pp 3138-3144, issn 0006-4971Article

Oral-dental findings in dyskeratosis congenitaYAVUZYILMAZ, E; YAMALIK, N; YETGIN, S et al.Journal of oral pathology & medicine. 1992, Vol 21, Num 6, pp 280-284, issn 0904-2512Article

Dyskeratosis congenita associated with elevated fetal hemoglobin, X-linked ocular albinism, and juvenile-onset diabetes mellitusREICHEL, M; GRIX, A. C; ISSEROFF, R. R et al.Pediatric dermatology. 1992, Vol 9, Num 2, pp 103-106, issn 0736-8046Conference Paper

Dyskeratosis congenita in a girl simulating chronic graft-vs-host diseaseLING, N. S; FENSKE, N. A; JULIUS, R. L et al.Archives of dermatology (1960). 1985, Vol 121, Num 11, pp 1424-1428, issn 0003-987XArticle

Bone marrow failure in dyskeratosis congenitaHANADA, T; ABE, t; NAKAZAWA, M et al.Scandinavian journal of haematology. 1984, Vol 32, Num 5, pp 496-500, issn 0036-553XArticle

Inherited bone marrow failure syndromes in 2012 : PIH: Recent advances in genetic basis of childhood hemato-oncological diseasesSAKAGUCHI, Hirotoshi; NAKANISHI, Koji; KOJIMA, Seiji et al.International journal of hematology. 2013, Vol 97, Num 1, pp 20-29, issn 0925-5710, 10 p.Article

Inactivation of the Tumor Suppressor Genes Causing the Hereditary Syndromes Predisposing to Head and Neck Cancer via Promoter Hypermethylation in Sporadic Head and Neck CancersSMITH, Lan M; MITHANI, Suhail K; MYDLARZ, Wojciech K et al.ORL. 2010, Vol 72, Num 1, pp 44-50, issn 0301-1569, 7 p.Article

Identification of TINF2 gene mutations in adult Japanese patients with acquired bone marrow failure syndromesYAMAGUCHI, Hiroki; INOKUCHI, Koiti; TAKEUCHI, Junko et al.British journal of haematology. 2010, Vol 150, Num 6, pp 725-727, issn 0007-1048, 3 p.Article

Treatment of dyskeratosis congenita with granulocyte-macrophage colony-stimulating factor and erythropoietinERDURAN, Erol; HACISALIHOGLU, Sadan; OZORAN, Yavuz et al.Journal of pediatric hematology/oncology. 2003, Vol 25, Num 4, pp 333-335, issn 1077-4114, 3 p.Article

Dyskeratosis Congenita : A historical perspectiveWALNE, Amanda J; DOKAL, Inderjeet.Mechanisms of ageing and development. 2008, Vol 129, Num 1-2, pp 48-59, issn 0047-6374, 12 p.Article

DYSKERATOSIS CONGENITA (ZINSSER-ENGMAN-COLE-SYNDROM) UND FANCONI-ANAEMIE = DYSKERATOSE CONGENITALE (SYNDROME DE ZINSSER-ENGMAN-COLE) ET ANEMIE DE FANCONIKORZ R; WIENERT V; KNECHTEN H et al.1982; HAUTARTZ; ISSN 0017-8470; DEU; DA. 1982; VOL. 33; NO 2; PP. 112-114; ABS. ENG; BIBL. 17 REF.Article

DYSKERATOSIS CONGENITA: SURVIVAL, SISTER-CHROMATID EXCHANGE AND REPAIR FOLLOWING TREATMENTS WITH CROSSLINKING AGENTSKANO Y; FUJIWARA Y.1982; MUTAT. RES.; ISSN 0027-5107; NLD; DA. 1982; VOL. 103; NO 3-6; PP. 327-332; BIBL. 16 REF.Article

LA MALATTIA DI FANCONI-ZINSSER. = LA MALADIE DE FANCONI-ZINSSERLOVISETTO P; MAIRANO S; BIARESE V et al.1977; MINERVA MED.; ITAL.; DA. 1977; VOL. 68; NO 25; PP. 1685-1708; ABS. ANGL.; BIBL. 2 P.Article

Effects of dyskeratosis congenita mutations in dyskerin, NHP2 and NOP10 on assembly of H/ACA pre-RNPsTRAHAN, Christian; MARTEL, Caroline; DRAGON, François et al.Human molecular genetics (Print). 2010, Vol 19, Num 5, pp 793-802, issn 0964-6906, 10 p.Article

Dyskeratosis CongenitaSAVAGE, Sharon A; ALTER, Blanche P.Hematology/oncology clinics of North America. 2009, Vol 23, Num 2, issn 0889-8588, viii, 215-231 [16 p.]Article