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

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

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

Dyskératose congénitale de Zinsser-Engmancole = Dyskeratosis congenitaCAUSSADE, P; HEID, E.Les Nouvelles dermatologiques. 1986, Vol 5, Num 1, pp 10-12, issn 0752-5370Article

Anemia aplástica en disqueratosis congénita = Anémie aplasique dans la dyskératose congénitale = Aplastic anemia in congenital dyskeratosisDEL ANGEL GUEVARA, O; DORANTES-MESA, S; REDON-TAVERA, A et al.Boletín Médico del Hospital Infantil de México (Ed. española). 1986, Vol 43, Num 3, pp 176-180, issn 0539-6115Article

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

Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10WALNE, Amanda J; VULLIAMY, Tom; MARRONE, Anna et al.Human molecular genetics (Print). 2007, Vol 16, Num 13, pp 1619-1629, issn 0964-6906, 11 p.Article

Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenitaALTER, Blanche P; BAERLOCHER, Gabriela M; SAVAGE, Sharon A et al.Blood. 2007, Vol 110, Num 5, pp 1439-1447, issn 0006-4971, 9 p.Article

Dyskeratosis congenitaVULLIAMY, Tom; DOKAL, Inderjeet.Seminars in hematology. 2006, Vol 43, Num 3, pp 157-166, issn 0037-1963, 10 p.Article

Dyskeratosis congenita : a light microscopic and ultrastructural studyKAGOURA, M; MOROHASHI, M.EJD. European journal of dermatology. 1998, Vol 8, Num 5, pp 307-309, issn 1167-1122Article

Abnormal nails in a patient with severe anemiaLIMMER, R. L; ZUROWSKI, S. M; SWINFARD, R. W et al.Archives of dermatology (1960). 1997, Vol 133, Num 1, pp 97-98, issn 0003-987XArticle

Dyskeratosis congenita in an ethnic Chinese girlHO, C. L.-Y; CHONG, L.-Y.International journal of dermatology. 1996, Vol 35, Num 9, pp 659-660, issn 0011-9059Article

Dyskeratosis congenita showing usual interstitial pneumoniaIMOKAWA, S; SATO, A; CHIDA, K et al.Internal medicine (Tokyo. 1992). 1994, Vol 33, Num 4, pp 226-230, issn 0918-2918Article

Síndrome de Zinsser-Cole-Engman (disqueratosis congénita) = Zinsser-Cole-Engman syndrome (dyskeratosis congenita)CAMBIAGHI, S; GRIMALT, R; TADINI, G et al.Medicina cutánea ibero-latino-americana. 1994, Vol 22, Num 3, pp 155-158, issn 0210-5187Article

Heterozygote detection through bleomycin-induced G₂ chromatid breakage in Dyskeratosis congenita familiesYANA NING; YAN YONGSHAN; PAI, G. S et al.Cancer genetics and cytogenetics. 1992, Vol 60, Num 1, pp 31-34, issn 0165-4608Article

Lingual hyperkeratosis in dyskeratosis congenita : ultrastructural findingsMCKAY, G. S; OGDEN, G. R; CHISHOLM, D. M et al.Journal of oral pathology & medicine. 1991, Vol 20, Num 4, pp 196-199, issn 0904-2512, 4 p.Article

Abnormality of platelet size and T-lymphocyte proliferation in an autosomal recessive form of dyskeratosis congenitaJUNEJA, H. S; ELDER, F. F. B; GARDNER, F. H et al.European journal of haematology. 1987, Vol 39, Num 4, pp 306-310, issn 0902-4441Article

Neuropsychiatric Conditions Among Patients with Dyskeratosis Congenita: A Link with Telomere Biology?RACKLEY, Sandra; PAO, Maryland; SERATTI, Guillermo F et al.Psychosomatics (Washington, DC). 2012, Vol 53, Num 3, pp 230-235, issn 0033-3182, 6 p.Article

DYSKERATOSIS CONGENITA-TWO SIBLINGS WITH A NEW MISSENSE MUTATION IN THE DKC1 GENEDIAS COELHO, Joana; LESTRE, Sara; KAY, Teresa et al.Pediatric dermatology. 2011, Vol 28, Num 4, pp 464-466, issn 0736-8046, 3 p.Article

Dyskeratosis Congenita : Report of a Case with Emphasis on Gingival AspectsLOURENCO, Silvia V; BOGGIO, Paula A; FEZZI, Fernando A et al.Pediatric dermatology. 2009, Vol 26, Num 2, pp 176-179, issn 0736-8046, 4 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 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