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Volumn 69, Issue 2, 2003, Pages 180-181

Passwell syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMINOACIDURIA; ARTICLE; CASE REPORT; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; DWARFISM; FEMALE; HUMAN; MENTAL DEFICIENCY; PASSWELL SYNDROME; PRIMARY AMENORRHEA; SKIN ATROPHY; SKIN DISEASE; SYMPTOMATOLOGY;

EID: 33745964123     PISSN: 03786323     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (3)
  • 1
    • 58149413220 scopus 로고
    • A syndrome characterised by congenital ichthyosis with atrophy, mental retardation, dwarfism and generalised amino aciduria
    • PasswelI J, Ziprkowskin L, Katzelson D, et al. A syndrome characterised by congenital ichthyosis with atrophy, mental retardation, dwarfism and generalised amino aciduria. J Pediatr 1973; 82: 466 - 5471.
    • (1973) J Pediatr , vol.82 , pp. 466-5471
    • Passweli, J.1    Ziprkowskin, L.2    Katzelson, D.3
  • 2
    • 0019004678 scopus 로고
    • Lamellar ichthyosis, dwarfism, mental retardation and hair shaft abnormalities
    • Jorizzo JI, Crounse RG, Wheeler CE J. Lamellar ichthyosis, dwarfism, mental retardation and hair shaft abnormalities. J Am Acad Dermatol 1980;2:309-317.
    • (1980) J Am Acad Dermatol , vol.2 , pp. 309-317
    • Jorizzo, J.I.1    Crounse, R.G.2    Wheeler, C.E.J.3
  • 3
    • 0017325698 scopus 로고
    • Lchthyosis with unusual hair shaft abnormalities in siblings
    • Yesudian P Srinivas K. lchthyosis with unusual hair shaft abnormalities in siblings. BrJ Dermatol 1977; 96: 199 -203.
    • (1977) BrJ Dermatol , vol.96 , pp. 199-203
    • Yesudian, P.1    Srinivas, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.