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Volumn 130, Issue 12 I, 2003, Pages 1143-1145

KID syndrome: A cause of pachydermatoglyphia;KID syndrome: Une cause de pachydermatoglyphie

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL FEATURE; CONSANGUINITY; ECTODERMAL DYSPLASIA; ERYTHEMA; EYEBROW; EYELASH; FEMALE; HAND PALM; HEARING IMPAIRMENT; HUMAN; HYPERKERATOSIS; HYPOTRICHOSIS; INTEGUMENT; KERATODERMA; KNEE; OPHTHALMOLOGY; PACHYDERMATOGLYPHIA; PHYLOGENY; SCHOOL CHILD; SYNDROME KID;

EID: 0346334719     PISSN: 01519638     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (4)
  • 2
    • 84943429907 scopus 로고
    • Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomas
    • Grob JJ, Breton I, Bonafé JL, Sauvant-Ferdani M, Bonerandi JJ. Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomas. Arch Dermatol 1987;123:777-82.
    • (1987) Arch Dermatol , vol.123 , pp. 777-782
    • Grob, J.J.1    Breton, I.2    Bonafé, J.L.3    Sauvant-Ferdani, M.4    Bonerandi, J.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.