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Journal Abstract Search

90 related items for PubMed ID: 9656468

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  • 24. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis.
    Lefevre P, Rochat A, Bodemer C, Vabres P, Barrandon Y, de Prost Y, Garner C, Hovnanian A.
    Eur J Hum Genet; 2000 Apr; 8(4):273-9. PubMed ID: 10854110
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  • 27. Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A LIPH mutation.
    Kinoshita-Ise M, Kubo A, Sasaki T, Umegaki-Arao N, Amagai M, Ohyama M.
    Br J Dermatol; 2017 Jan; 176(1):138-144. PubMed ID: 27375176
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  • 28. Rex mutant in the Norway rat.
    Robinson R.
    J Hered; 1981 Jan; 72(2):131-2. PubMed ID: 7276514
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  • 29. Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin.
    Sprecher E, Bergman R, Richard G, Lurie R, Shalev S, Petronius D, Shalata A, Anbinder Y, Leibu R, Perlman I, Cohen N, Szargel R.
    Nat Genet; 2001 Oct; 29(2):134-6. PubMed ID: 11544476
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  • 30. Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis.
    Yun SK, Cho YG, Song KH, Hwang SR, Kim Yoon SJ, Choi KW, Kim HU, Park J.
    Int J Dermatol; 2014 Nov; 53(11):1358-61. PubMed ID: 24961381
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  • 31. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.
    Wali A, Chishti M, Ayub M, Yasinzai M, Kafaitullah, Ali G, John P, Ahmad W.
    Clin Genet; 2007 Jul; 72(1):23-9. PubMed ID: 17594396
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  • 32. A missense mutation within the helix initiation motif of the keratin K71 gene underlies autosomal dominant woolly hair/hypotrichosis.
    Fujimoto A, Farooq M, Fujikawa H, Inoue A, Ohyama M, Ehama R, Nakanishi J, Hagihara M, Iwabuchi T, Aoki J, Ito M, Shimomura Y.
    J Invest Dermatol; 2012 Oct; 132(10):2342-2349. PubMed ID: 22592156
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  • 35. Phenotypic observations in "hypotrichosis with juvenile macular dystrophy" (recessive CDH3 mutations).
    Khan AO, Bolz HJ.
    Ophthalmic Genet; 2016 Sep; 37(3):301-6. PubMed ID: 26885695
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  • 36. A novel deletion mutation in P2RY5/LPA(6) gene cause autosomal recessive woolly hair with hypotrichosis.
    Horev L, Saad-Edin B, Ingber A, Zlotogorski A.
    J Eur Acad Dermatol Venereol; 2010 Jul; 24(7):858-9. PubMed ID: 20015179
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  • 37. Phenotypic diversity and mutation spectrum in hypotrichosis with juvenile macular dystrophy.
    Indelman M, Hamel CP, Bergman R, Nischal KK, Thompson D, Surget MO, Ramon M, Ganthos H, Miller B, Richard G, Lurie R, Leibu R, Russell-Eggitt I, Sprecher E.
    J Invest Dermatol; 2003 Nov; 121(5):1217-20. PubMed ID: 14708629
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  • 39. Progressive patterned scalp hypotrichosis, with wiry hair, onycholysis, and intermittently associated cleft lip and palate: clinical and genetic distinction from Marie Unna.
    Green J, Fitzpatrick E, de Berker D, Forrest SM, Sinclair RD.
    J Investig Dermatol Symp Proc; 2003 Jun; 8(1):121-5. PubMed ID: 12895008
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  • 40. A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp.
    Nahum S, Morice-Picard F, Taieb A, Sprecher E.
    Clin Exp Dermatol; 2011 Mar; 36(2):188-94. PubMed ID: 21070332
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