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• 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. Spritz RA, et al. Am J Hum Genet. 1991 Feb;48(2):318-24. Am J Hum Genet. 1991. PMID: 1899321 Free PMC article.
• A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.

  Giebel LB, Strunk KM, King RA, Hanifin JM, Spritz RA. Giebel LB, et al. Proc Natl Acad Sci U S A. 1990 May;87(9):3255-8. doi: 10.1073/pnas.87.9.3255. Proc Natl Acad Sci U S A. 1990. PMID: 1970634 Free PMC article.
• A single base insertion in the putative transmembrane domain of the tyrosinase gene as a cause for tyrosinase-negative oculocutaneous albinism.

  Chintamaneni CD, Halaban R, Kobayashi Y, Witkop CJ Jr, Kwon BS. Chintamaneni CD, et al. Proc Natl Acad Sci U S A. 1991 Jun 15;88(12):5272-6. doi: 10.1073/pnas.88.12.5272. Proc Natl Acad Sci U S A. 1991. PMID: 1711223 Free PMC article.
• PCR detection of a TaqI polymorphism at the CCAATT box of the human tyrosinase (TYR) gene.

  Oetting WS, Roed CM, Mentink MM, King RA. Oetting WS, et al. Nucleic Acids Res. 1991 Oct 25;19(20):5800. doi: 10.1093/nar/19.20.5800-a. Nucleic Acids Res. 1991. PMID: 1682887 Free PMC article. No abstract available.
• Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: linkage analysis of 111 families by an international consortium.

  Foroud T, Wei S, Ziv Y, Sobel E, Lange E, Chao A, Goradia T, Huo Y, Tolun A, Chessa L, Charmley P, Sanal O, Salman N, Julier C, Concannon P, McConville C, Taylor AM, Shiloh Y, Lange SK, Gatti RA. Foroud T, et al. Am J Hum Genet. 1991 Dec;49(6):1263-79. Am J Hum Genet. 1991. PMID: 1746555 Free PMC article.