CiteULike: Archaeogenetics's Stevens:G [2 articles]

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	An intragenic deletion of the P gene is the common mutation causing tyrosinase-positive oculocutaneous albinism in southern African Negroids. [My Copy] Am J Hum Genet, Vol. 56, No. 3. (March 1995), pp. 586-591. by G. Stevens, J. van Beukering, T. Jenkins, M. Ramsay posted to 27kb-del africa albinism haplotypes oca2 sub-saharan_africa by Archaeogenetics on 2007-10-18 20:31:25 as
	Oculocutaneous albinism (OCA2) in sub-Saharan Africa: distribution of the common 2.7-kb P gene deletion mutation. [My Copy] Hum Genet, Vol. 99, No. 4. (April 1997), pp. 523-527. by G. Stevens, M. Ramsay, T. Jenkins posted to 27kb-del africa albinism oca2 sub-saharan_africa by Archaeogenetics on 2007-10-18 20:11:18 as

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