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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

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 ZINSSER-COLE-ENGMANN FORM WITH ABNORMAL KARYOTYPE = DYSKERATOSE CONGENITALE, SYNDROME DE ZINSSER-COLE-ENGMANN AVEC CARYOTYPE ANORMALROBLEDO AGUILAR A; GOMEZ F; TOJO SIERRA R et al.1974; DERMATOLOGICA; SUISSE; DA. 1974; VOL. 148; NO 2; PP. 98-103; BIBL. 9 REF.Article

ZINSSER-ENGMAN - COLE-SYNDROM = SYNDROME DE ZINSSER. ENGMAN-COLESCHMIDT JB; GEBHART W.1983; HAUTARZT; ISSN 0017-8470; DEU; DA. 1983; VOL. 34; NO 6; PP. 286-288; ABS. ENG; BIBL. 8 REF.Article

DYSKERATOSE DE ZINSSER COLE ENGMANKOLYADENKO VG; LEVKOVSKIJ NM; SHUPEN'KO NM et al.1979; VEST. DERMATOL. VENEROL.; SUN; DA. 1979; NO 2; PP. 36-40; ABS. ENG; BIBL. 1 P.Article

DYSKERATOSIS CONGENITAGARTSIDE JM.1978; BRIT. J. DERMATOL. SUPPL.; GBR; DA. 1978; VOL. 99; NO 16; PP. 31Article

THROMBOCYTOPENIA: FIRST SYMPTOM IN A PATIENT WITH DYSKERATOSIS CONGENITADE BOECK K; DEGREEF H; VERWILGHEN R et al.1981; PEDIATRICS (EVANSTON); ISSN 0031-4005; USA; DA. 1981; VOL. 67; NO 6; PP. 898-903; BIBL. 24 REF.Article

POIKILODERMIE. PIGMENTATION. PACHYONYCHIE. PANCYTOPENIE (VARIANT DE LA DYSKERATOSE CONGENITALE OU ENTITE NOUVELLE).LARREGUE M; DOMMERGUES J; COURTECUISSE P et al.1976; BULL. SOC. FR. DERMATOL. SYPHILIGR.; FR.; DA. 1976; VOL. 83; NO 4; PP. 254-255Article

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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 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

DYSKERATOSIS CONGENITA: RADIOLOGIC FEATURESKELLY TE; STELLING CB.1982; PEDIATR. RADIOL.; ISSN 0301-0449; DEU; DA. 1982; VOL. 12; NO 1; PP. 31-36; BIBL. 8 REF.Article

SYNDROME DE ZINSSER-COLE-ENGMANN. FORME COMPLETE AVEC ATTEINTE HEMATOLOGIQUE SEVERE TRAITEE PAR GREFFE DE MOELLE OSSEUSE ALLOGENIQUELEMARCHAND VENENCIE F; GLUCKMAN E; DEVERGIE A et al.1982; ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE; ISSN 0151-9638; FRA; DA. 1982; VOL. 109; NO 9; PP. 783-784; BIBL. 2 REF.Article

NEW FORMS OF DISEASES WITH DNA REPAIR DEFECTSROBBINS JH.1979; PHOTOCHEM. AND PHOTOBIOL.; GBR; DA. 1979; VOL. 30; NO 6; PP. 739-741; BIBL. 28 REF.Article

SYNDROME DE ZINSSER-COLE-ENGMAN. L'INTERET DE L'AUTOGREFFE DE CELLULES SOUCHES HEMATOPOIETIQUESBERTRAND AM; PLOUVIER E; HERVE P et al.1981; MED. INFANT.; ISSN 0025-6773; GBR; DA. 1981; VOL. 88; NO 5; PP. 593-600; 6 P.; BIBL. 25 REF.Article

DYSKERATOSE CONGENITALE DE ZINSSER-COLE-ENGMAN CHEZ DEUX FRERESLORETTE G; GUEROIS M; ARBEILLE BRASSART B et al.1980; ANN. DERMATOL. VENEREOL.; ISSN 0151-9638; FRA; DA. 1980; VOL. 107; NO 8-9; PP. 799-805; ABS. ENG; BIBL. 36 REF.Article

DYSKERATOSIS CONGENITA: TWO EXAMPLES OF THIS MULTISYSTEM DISORDERWOMER R; CLARK JE; WOOD P et al.1983; PEDIATRICS (EVANSTON); ISSN 0031-4005; USA; DA. 1983; VOL. 71; NO 4; PP. 603-609; BIBL. 43 REF.Article

DEFICIT OF CELL-MEDIATED IMMUNITY, CHROMOSOMAL ALTERATIONS AND DEFECTIVE DNA IN A CASE OF DYSKERATOSIS CONGENITAGIANNETTI A; SEIDENARI S.1980; DERMATOLOGICA; CHE; DA. 1980; VOL. 160; NO 2; PP. 113-117; BIBL. 14 REF.Article

UNE ASSOCIATION INEDITE: DYSKERATOSE DE ZINSSER-COLE-ENGMANN, SYNDROME DE KLIPPEL-FEIL ET MALFORMATION DE SPRENGELMALEVILLE J; LE ROY JM; DIARD F et al.1980; ANN. DERMATOL. VENEREOL.; ISSN 0151-9638; FRA; DA. 1980; VOL. 107; NO 12; PP. 1207-1211; BIBL. 14 REF.Article

DAS ZINSSER-COLE-ENGMAN. SYNDROM EIN BEITRAG ZU DEN KONGENITALEN POIKILODERMIEN, ZUGLEICH EIN BEITRAG ZU DEN FAMILIAEREN PANZYTOPENIEN = LE SYNDROME DE ZINSSER-COLI-ENGMAN. UNE CONTRIBUTION AUX POIKILODERMIES CONGENITALES ET AUX PANCYTOPENIES FAMILIALESRODERMUND OE; HAUSMANN D; HAUSMANN G et al.1979; Z. HAUTKRANKH.; DEU; DA. 1979; VOL. 54; NO 7; PP. 273-286; BIBL. 75 REF.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