CiteULike: Archaeogenetics's Jenkins:T [4 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
	Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes. [My Copy] Proc Natl Acad Sci U S A, Vol. 97, No. 12. (6 June 2000), pp. 6769-6774. by M. F. Hammer, A. J. Redd, E. T. Wood, et al.M. R. Bonner, H. Jarjanazi, T. Karafet, S. Santachiara-Benerecetti, A. Oppenheim, M. A. Jobling, T. Jenkins, H. Ostrer, B. Bonne-Tamir posted to ashkenazi ethiopian jews kurdish near_easternyemenite north_african roman y by Archaeogenetics on 2006-08-16 13:19:19 as along with 1 person Gershom
	High polymorphism at the human melanocortin 1 receptor locus. [My Copy] Genetics, Vol. 151, No. 4. (April 1999), pp. 1547-1557. by B. K. Rana, D. Hewett-Emmett, L. Jin, et al.B. H. Chang, N. Sambuughin, M. Lin, S. Watkins, M. Bamshad, L. B. Jorde, M. Ramsay, T. Jenkins, W. H. Li posted to archaic autosomal mc1r melanocortin by Archaeogenetics on 2006-05-27 00:37:02 as

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microcephalin	4
mongolia	4
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slavery	2
solomon_islands	2
south_america	2
spanish	2
sub-saharan	2
survey	2
synonymous	2
t3394c	2
tanzania	2

Archaeogenetics's Jenkins:T [4 articles] Export

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