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Volumn 58, Issue 2, 2003, Pages 192-193

Intestinal subocclusion due to congenital trichobezoar [2];Suboclusión intestinal por tricobezoar congénito

Author keywords

[No Author keywords available]

Indexed keywords

ABDOMINAL DISTENSION; ALOPECIA; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; DIFFERENTIAL DIAGNOSIS; HUMAN; INTESTINE OBSTRUCTION; LETTER; NEWBORN; TRICHOBEZOAR;

EID: 0037731548     PISSN: 16954033     EISSN: None     Source Type: Journal    
DOI: 10.1157/13042975     Document Type: Letter
Times cited : (1)

References (10)
  • 4
    • 0028063912 scopus 로고
    • Isolated congenital atrichia in an Omani kindred
    • Kenue RK, Al-dhafri KS. Isolated congenital atrichia in an Omani kindred. Dermatol 1994;188:72-5.
    • (1994) Dermatol , vol.188 , pp. 72-75
    • Kenue, R.K.1    Al-dhafri, K.S.2
  • 6
    • 0031723522 scopus 로고    scopus 로고
    • Congenital atrichia in five Arab Palestinian families resulting from a deletion mutation in the human hairless gene
    • Zlotogorsky A, Ahmad W, Christiano AM. Congenital atrichia in five Arab Palestinian families resulting from a deletion mutation in the human hairless gene. Hum Genet 1998;103:400-4.
    • (1998) Hum Genet , vol.103 , pp. 400-404
    • Zlotogorsky, A.1    Ahmad, W.2    Christiano, A.M.3
  • 7
    • 0019186475 scopus 로고
    • Analysis of hair from alopecia congenita
    • Baden HP, Kubilus J. Analysis of hair from alopecia congenita. J Am Acad Dermatol 1980;3:623-6.
    • (1980) J Am Acad Dermatol , vol.3 , pp. 623-626
    • Baden, H.P.1    Kubilus, J.2
  • 8
    • 0032231885 scopus 로고    scopus 로고
    • A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travelers
    • Ahmad W, et al. A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travelers. Am J Hum Genet 1998;63:984-91.
    • (1998) Am J Hum Genet , vol.63 , pp. 984-991
    • Ahmad, W.1
  • 9
    • 0033390792 scopus 로고    scopus 로고
    • The molecular basis of congenital atrichia in humans and mice: Mutations in the hairless gene
    • Ahmad W, Panteleyev AA, Christiano AM. The molecular basis of congenital atrichia in humans and mice: Mutations in the hairless gene. J Investig Dermatol Symp Proc 1999;4:240-3.
    • (1999) J Investig Dermatol Symp Proc , vol.4 , pp. 240-243
    • Ahmad, W.1    Panteleyev, A.A.2    Christiano, A.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.