Universal dyschromatosis: A family study;Dyschromatose universelle: Une observation familiale

Annales de Dermatologie et de Venereologie

Volumn 125, Issue 10, 1998, Pages 700-704

  Schoenlaub, P ^a   Leroy, J P ^a   Dupre D ^b   Chaboche, C ^a   Plantin, P ^a  

^a Hopital Laennec   (France)

^b BREST UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL FEATURE; FEMALE; GENETIC SUSCEPTIBILITY; HERITABILITY; HUMAN; HYPERPIGMENTATION; HYPOPIGMENTATION; PIGMENT DISORDER; SCHOOL CHILD; SKIN BIOPSY;

ADULT; CHILD; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; MALE; PEDIGREE; PIGMENTATION DISORDERS; SKIN; XERODERMA PIGMENTOSUM;

EID: 0031727494     PISSN: 01519638     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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