메뉴 건너뛰기




Volumn 19, Issue 4, 1988, Pages 642-655

Congenital dyschromia with erythrocyte, platelet, and tryptophan metabolism abnormalities

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CONGENITAL DISORDER; ERYTHROCYTE; FEMALE; HISTOLOGY; HUMAN; HYPERPIGMENTATION; HYPOPIGMENTATION; PRESCHOOL CHILD; PRIORITY JOURNAL; THROMBOCYTE; TRYPTOPHAN METABOLISM; ULTRASTRUCTURE;

EID: 0023680504     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0190-9622(88)70218-2     Document Type: Article
Times cited : (11)

References (42)
  • 8
    • 0014680921 scopus 로고
    • 3H assay for tyrosinase development in skin of newborn hamsters
    • (1969) Science , vol.164 , pp. 838-840
    • Pomerantz, SH1
  • 18
    • 0021889048 scopus 로고
    • The Hermansky-Pudlak syndrome: report of three cases and review of pathophysiology and management considerations
    • (1985) Medicine , vol.64 , pp. 192-202
    • Depinho, RA1    Kaplan, KL2
  • 25
    • 0013935887 scopus 로고
    • Melanosomes in phagocytic vacuoles in Langerhans cells: electronmicroscopy of keratin-stripped human epidermis
    • (1966) J Cell Biol , vol.30 , pp. 417-423
    • Mishima, Y1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.