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kw.\*:("Disqueratosis congénita Zinsser Engman Cole")

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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

Dyskeratosis congenita : clinical and genetic heterogeneity : report of a new case and review of the literatureDRACHTMAN, R. A; ALTER, B. P.The American journal of pediatric hematology/oncology. 1992, Vol 14, Num 4, pp 297-304, issn 0192-8562Article

Dyskeratosis congenita fibroblasts are abnormal and have unbalanced chromosomal rearrangementsDOKAL, I; BUNGEY, J; WILLIAMSON, P et al.Blood. 1992, Vol 80, Num 12, pp 3090-3096, issn 0006-4971Article

What syndrome is this characteristic of ?MALLORY, S. B; KRAFCHIK, B. R.Pediatric dermatology. 1991, Vol 8, Num 1, pp 81-83, issn 0736-8046, 3 p.Article

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

Dystkeratosis congenita: unusual presenting features within a kindredFORNI, G. L; MELEVENDI, C; JAPPEELI, S et al.Pediatric hematology and oncology. 1993, Vol 10, Num 2, pp 145-149, issn 0888-0018Article

Cytogenetic studies of skin fibroblast cultures from a karyotypically normal female with dyskeratosis congenitaKEHRER, H; KEHRER, H et al.KRONE, W; KEHRER, H; KEHRER, H et al.KRONE, W; Clinical genetics. 1992, Vol 41, Num 3, pp 129-134, issn 0009-9163Article

Dyskeratosis congenita (Zinsser-Cole-Engman syndrome) : an autopsy case presenting with rectal carcinoma, non-cirrhotic portal hypertension, and Pneumocystis carinii pneumoniaKAWAGUCHI, K; SAKAMAKI, H; ONOZAWA, Y et al.Virchows Archiv. A, Pathological anatomy and histopathology. 1990, Vol 417, Num 3, pp 247-253, issn 0174-7398Article

Disceratose congênita. Syndrome de Zinsser, Engman e Cole = Dyskératose congénitale. Syndrome de Zinsser Engman et Cole = Congenital dyskeratosis. Zinsser Engman and Cole syndromeBELO DOS SANTOS, I; RICARDO SABINO, J; EDUARDO DA SILVA, R et al.Anais brasileiros de dermatologia. 1987, Vol 62, Num 2, pp 115-116, issn 0365-0596Article

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 congenitaRÖTH, Alexander; BAERLOCHER, Gabriela M.British journal of haematology. 2008, Vol 141, Num 4, pp 412-412, issn 0007-1048, 1 p.Article

Dyskeratosis congenita : Its connections with oral and maxillofacial surgerySABESAN, T; BAHEERATHAN, N. N; ILANKOVAN, V et al.British journal of oral & maxillofacial surgery. 2007, Vol 45, Num 2, pp 156-158, issn 0266-4356, 3 p.Article

Dyskerin localizes to the nucleolus and its mislocalization is unlikely to play a role in the pathogenesis of dyskeratosis congenitaHEISS, N. S; GIROD, A; SALOWSKY, R et al.Human molecular genetics (Print). 1999, Vol 8, Num 13, pp 2515-2524, issn 0964-6906Article

Disqueratosis congénita: un padecimiento premaligno. Comunicación de cuatro casos con alteraciones sistémicas = Dyskeratosis congenita:A premalignant condition.Communication of four cases with systemic involvementHERRERA-NAVARRO, M; DURAN, C; TAMAYO, L et al.Medicina cutánea ibero-latino-americana. 1995, Vol 23, Num 2, pp 61-64, issn 0210-5187Article

Dyskeratosis congenita preseded by severe aplastic anemia : report of one caseCHI-YUH KUO; DONG-TSAMM LIN; WEN-MIN TUU et al.Xiaoér keyi xuéhuì zázhì. 1989, Vol 30, Num 5, pp 337-341, issn 0001-6578, 5 p.Article

Dyskeratosis congenitaDAVIDSON, H. R; CONNOR, J. M.Journal of medical genetics. 1988, Vol 25, Num 12, pp 843-846, issn 0022-2593Article

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

Anomalies du complexe de la télomérase en pathologie hématologique = Telomerase complex defects in hematological diseasesMARIE-EGYPTIENNEL, Delphine T; AUTEXIER, Chantai.Hématologie (Montrouge). 2006, Vol 12, Num 4, pp 267-273, issn 1264-7527, 7 p.Article

Anomalies unguéales et fibrose pulmonaire diffuse = Dyskeratosis congenita and diffuse lung fibrosisHAFSAOUI, C; MAHAMMEDI, H; MANZONI, P et al.La Revue de médecine interne (Paris). 2004, Vol 25, Num 5, pp 395-396, issn 0248-8663, 2 p.Article

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