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Volumn 17, Issue 8, 2011, Pages

Dyschromatosis universalis hereditaria in an African American male

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AFRICAN AMERICAN; ARTICLE; CASE REPORT; CONGENITAL DISORDER; DYSCHROMATOSIS UNIVERSALIS HEREDITARIA; GENODERMATOSIS; HISTOPATHOLOGY; HUMAN; HYPERPIGMENTATION; HYPOPIGMENTATION; MALE; MEDICAL HISTORY; NORTH AMERICA; PRURITUS; SKIN BIOPSY; SKIN DISCOLORATION;

EID: 80051765737     PISSN: 10872108     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (14)
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    • A previously undescribed anomaly of pigmentation dyschromatosis universalis hereditaria
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    • Ichigawa, T.1    Hiraga, Y.2
  • 2
    • 0000309721 scopus 로고
    • Genetical studies on skin diseases. VII. Dyschromatosis universalis hereditaria in five generations
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    • Suenaga, M.1
  • 3
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    • (2009) Int J Dermatol , vol.48 , Issue.7 , pp. 749-750
    • Yusuf, S.M.1    Mijinyawa, M.S.2    Maiyaki, M.B.3    Mohammed, A.Z.4
  • 4
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    • Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation
    • [PubMed]
    • Nuber UA, Tinschert S, Mundlos S, and Haußer I. Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation. Am J Med Genet A 2004;125(3):261-266. [PubMed]
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    • Nuber, U.A.1    Tinschert, S.2    Mundlos, S.3    Haußer, I.4
  • 5
    • 0036862123 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria: Report of a case and review of the literature
    • [PubMed]
    • Al Hawsawi K, Al Aboud K, Ramesh V, and Al Aboud D. Dyschromatosis universalis hereditaria: report of a case and review of the literature. Pediatr Dermatol 2002; 19:523-526. [PubMed]
    • (2002) Pediatr Dermatol , vol.19 , pp. 523-526
    • Al Hawsawi, K.1    Al Aboud, K.2    Ramesh, V.3    Al Aboud, D.4
  • 8
    • 79953065223 scopus 로고    scopus 로고
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    • Feb 15, [PubMed]
    • Udayashankar C and Nath, AK. Dyschromatosis universalis hereditaria: A case report. Dermatol Online Journal 2011 Feb 15; 17(2): 2. [PubMed]
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    • Udayashankar, C.1    Nath, A.K.2
  • 9
    • 33646033001 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family
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    • (2006) Europ. Acad. Derm. Venerol. , vol.18 , pp. 628-629
    • Bukhari, I.A.1    El-Harith, E.A.2    Stuhrmann, M.3
  • 11
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    • Dyschromatosis universalis hereditaria: An electron microscopic examination
    • Mar, [PubMed]
    • Kim NS, Im S, Kim SC. Dyschromatosis universalis hereditaria: an electron microscopic examination. J Dermatol. 1997 Mar;24(3):161-4. [PubMed]
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  • 13
    • 0042242613 scopus 로고    scopus 로고
    • A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2
    • [PubMed]
    • Xing Q, Wang M, Chen X, Feng G, Ji H, Yang J, Gao J, Qin W, Qian X, Wu S, and He L. A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2. Am J Hum Genet. 73: 377-382, 2003. [PubMed]
    • (2003) Am J Hum Genet. , vol.73 , pp. 377-382
    • Xing, Q.1    Wang, M.2    Chen, X.3    Feng, G.4    Ji, H.5    Yang, J.6    Gao, J.7    Qin, W.8    Qian, X.9    Wu, S.10    He, L.11
  • 14
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    • Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria
    • [PubMed]
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    • Miyamura, Y.1    Suzuki, T.2    Kono, M.3    Inagaki, K.4    Ito, S.5    Suzuki, N.6    Tomita, Y.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.