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Volumn 27, Issue 8, 2002, Pages 654-656

Hereditary hypotrichosis simplex: Report of a family

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; FEMALE; GENETIC DISORDER; GENODERMATOSIS; HAIR ANALYSIS; HAIR FOLLICLE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPOTRICHOSIS; MALE; PRIORITY JOURNAL; SCANTY HAIR; SKIN BIOPSY; SKIN DISEASE; SKIN EXAMINATION; SKIN INFLAMMATION; SWEAT GLAND;

EID: 0036456836     PISSN: 03076938     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2230.2002.01088.x     Document Type: Article
Times cited : (7)

References (14)
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    • De Berker, D.A.R.1
  • 2
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    • Hereditary hypotrichosis simplex of the scalp: Evidence for autosomal dominant inheritance
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  • 3
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    • Hereditary hypotrichosis simplex of the scalp
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    • Khon, G.1    Metzker, A.2
  • 4
    • 0025852986 scopus 로고
    • Hereditary hypotrichosis of the scalp
    • Hess RO, Uno H. Hereditary hypotrichosis of the scalp. Am J Med Genet 1991; 39: 125-9.
    • (1991) Am J Med Genet , vol.39 , pp. 125-129
    • Hess, R.O.1    Uno, H.2
  • 5
    • 0025734237 scopus 로고
    • Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations
    • Ibsen HH, Clemmensen OJ, Brandrup F. Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations. Acta Derm Venereol 1991; 7: 349-51.
    • (1991) Acta Derm Venereol , vol.7 , pp. 349-351
    • Ibsen, H.H.1    Clemmensen, O.J.2    Brandrup, F.3
  • 8
    • 0032838974 scopus 로고    scopus 로고
    • A sporadic case of congenital hypotrichosis simplex of the scalp: Difficulties in diagnosis and classification
    • Cambiaghi S, Barbareschi M. A sporadic case of congenital hypotrichosis simplex of the scalp: Difficulties in diagnosis and classification. Pediatr Dermatol 1999; 16: 301-4.
    • (1999) Pediatr Dermatol , vol.16 , pp. 301-304
    • Cambiaghi, S.1    Barbareschi, M.2
  • 9
    • 0033941849 scopus 로고    scopus 로고
    • A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3
    • Betz RC, Lee YA, Bygum A et al. A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3. Am J Hum Genet 2000; 66: 1979-83.
    • (2000) Am J Hum Genet , vol.66 , pp. 1979-1983
    • Betz, R.C.1    Lee, Y.A.2    Bygum, A.3
  • 10
    • 0018596307 scopus 로고
    • Hereditary hypotrichosis: A previously undescribed syndrome
    • Bentley-Phillips B, Grace HJ. Hereditary hypotrichosis: A previously undescribed syndrome. Br J Dermatol 1979; 101: 331-9.
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    • Bentley-Phillips, B.1    Grace, H.J.2
  • 11
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    • Baumer A, Belli S, Trueb RM, Schinzel A. An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32 - p11.23 in an Italian family. Eur J Hum Genet 2000; 8: 443-8.
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    • Baumer, A.1    Belli, S.2    Trueb, R.M.3    Schinzel, A.4
  • 12
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    • Missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish traveller
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    • Ahmed, W.1    Irvine, A.D.2    Lam, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.