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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

90 related items for PubMed ID: 9656468

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  • 44. A missense mutation in CDH3, encoding P-cadherin, causes hypotrichosis with juvenile macular dystrophy.
    Indelman M, Bergman R, Lurie R, Richard G, Miller B, Petronius D, Ciubutaro D, Leibu R, Sprecher E.
    J Invest Dermatol; 2002 Nov; 119(5):1210-3. PubMed ID: 12445216
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  • 49. 'Atrichosis', a new hairless gene with cyst formation in rats.
    Ohno T, Yoshida H.
    Experientia; 1981 Feb 15; 37(2):126-7. PubMed ID: 7238735
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  • 52. A novel mutation in lysophosphatidic acid receptor 6 gene in autosomal recessive hypotrichosis and evidence for a founder effect.
    Azhar A, Tariq M, Baig SM, Dahl N, Klar J.
    Eur J Dermatol; 2012 Feb 15; 22(4):464-6. PubMed ID: 22531990
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  • 53. A novel deletion mutation in the LPAR6 gene underlies autosomal recessive woolly hair with hypotrichosis.
    Liu LH, Chen G, Wang JW, Liu SX, Wang JB, Zhou FS, Zhu J, Sun LD, Gao M, Wang PG, Yang S, Zhang XJ.
    Clin Exp Dermatol; 2013 Oct 15; 38(7):796-8. PubMed ID: 23773027
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  • 54. Genetic study of osteopetrosis in the Norway rat.
    Moutier R, Toyama K, Charrier MF.
    J Hered; 1974 Oct 15; 65(6):373-5. PubMed ID: 4615115
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  • 57. A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families.
    Nahum S, Pasternack SM, Pforr J, Indelman M, Wollnik B, Bergman R, Nöthen MM, König A, Khamaysi Z, Betz RC, Sprecher E.
    Arch Dermatol Res; 2009 Jun 15; 301(5):391-3. PubMed ID: 18820939
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  • 58. Novel mutation in LIPH in a Lebanese patient with autosomal recessive woolly hair/hypotrichosis.
    Sleiman MB, Sleiman MB, Abbas O, Btadini W, Najjar T, Tofaili M, Chedraoui A, Khalil S, Kibbi AG, Kurban M.
    J Dermatol; 2015 Aug 15; 42(8):822-4. PubMed ID: 26046953
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  • 59. Genetic factors involved in heterochromia in the Norway rat.
    Macy RM, Stanley AJ, Gumbreck LG.
    J Hered; 1972 Aug 15; 63(4):189-90. PubMed ID: 5075898
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  • 60. Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan.
    Takeichi T, Tanahashi K, Taki T, Kono M, Sugiura K, Akiyama M.
    Br J Dermatol; 2017 Jul 15; 177(1):290-292. PubMed ID: 27641630
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