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Volumn 159, Issue 10, 2000, Pages 745-749

Cutis tricolor: Congenital hyper- and hypopigmented lesions in a background of normal skin with and without associated systemic features: Further expansion of the phenotype

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; BIRTH DEFECT; CASE REPORT; CHILD; CUTIS TRICOLOR; DIAGNOSTIC IMAGING; FACE DYSMORPHIA; HUMAN; HYPERPIGMENTATION; HYPOPIGMENTATION; MALE; MUSCULOSKELETAL DISEASE; PHENOTYPE; PIGMENT DISORDER; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER; SKIN PIGMENTATION; WHITE MATTER;

EID: 0033818003     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/PL00008339     Document Type: Article
Times cited : (59)

References (22)
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    • 0007959171 scopus 로고    scopus 로고
    • Genetic skin disorders. Oxford University Press, New York
    • (1997)
    • Sybert, V.P.1
  • 19
    • 0031744843 scopus 로고    scopus 로고
    • Gross deletions of the neurofibromatosis type 1 gene (Nfl) are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay
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    • (1999) Am J Med Genet , vol.85 , pp. 323-364


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.