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Journal Abstract Search


154 related items for PubMed ID: 1409411

  • 21.
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  • 22. Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism.
    King RA, Mentink MM, Oetting WS.
    Mol Biol Med; 1991 Feb; 8(1):19-29. PubMed ID: 1943686
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  • 23. Temperature-sensitive tyrosinase associated with peripheral pigmentation in oculocutaneous albinism.
    King RA, Townsend D, Oetting W, Summers CG, Olds DP, White JG, Spritz RA.
    J Clin Invest; 1991 Mar; 87(3):1046-53. PubMed ID: 1900307
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  • 28. OCA1 in different ethnic groups of india is primarily due to founder mutations in the tyrosinase gene.
    Chaki M, Sengupta M, Mukhopadhyay A, Subba Rao I, Majumder PP, Das M, Samanta S, Ray K.
    Ann Hum Genet; 2006 Sep; 70(Pt 5):623-30. PubMed ID: 16907708
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  • 30. Technical advances in prenatal diagnosis of tyrosinase-negative oculocutaneous albinism.
    Shimizu H.
    Acta Derm Venereol; 1997 Jan; 77(1):10-3. PubMed ID: 9059668
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  • 32. One-allele system in the Korean for MboI-RFLP in exon 1 of the human tyrosinase (TYR) gene.
    Kim DK, Kang KH, Choi IJ.
    J Dermatol Sci; 2000 Sep; 24(1):1-3. PubMed ID: 10960773
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  • 33. Homozygous tyrosinase gene mutation in an American black with tyrosinase-negative (type IA) oculocutaneous albinism.
    Spritz RA, Strunk KM, Hsieh CL, Sekhon GS, Francke U.
    Am J Hum Genet; 1991 Feb; 48(2):318-24. PubMed ID: 1899321
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  • 34.
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  • 35. Molecular basis of oculocutaneous albinism.
    Oetting WS, King RA.
    J Invest Dermatol; 1994 Nov; 103(5 Suppl):131S-136S. PubMed ID: 7963676
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  • 36. The nature of tyrosinase isozymes.
    Tsukamoto K, Jiménez M, Hearing VJ.
    Pigment Cell Res; 1992 Nov; Suppl 2():84-9. PubMed ID: 1409443
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  • 37. DNA-based carrier detection and prenatal diagnosis of tyrosinase-negative oculocutaneous albinism (OCA1A).
    Falik-Borenstein TC, Holmes SA, Borochowitz Z, Levin A, Rosenmann A, Spritz RA.
    Prenat Diagn; 1995 Apr; 15(4):345-9. PubMed ID: 7617575
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  • 38. Novel human pathological mutations. Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
    Saxena R, Verma IC.
    Hum Genet; 2010 Apr; 127(4):488. PubMed ID: 21491619
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  • 39. Cloning and sequence analysis of the tyrosinase gene from a patient with tyrosinase-positive oculocutaneous albinism.
    Matsunaga J, Takeda A, Tomita Y, Hara M, Shibahara S, Tagami H.
    J Dermatol Sci; 1992 May; 3(3):181-5. PubMed ID: 1498098
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  • 40. R278TER and P431L mutations of the tyrosinase gene exist in Japanese patients with tyrosinase-negative oculocutaneous albinism.
    Matsunaga J, Dakeishi M, Shimizu H, Tomita Y.
    J Dermatol Sci; 1996 Nov; 13(2):134-9. PubMed ID: 8953413
    [Abstract] [Full Text] [Related]


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