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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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t122p36q13	1
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t3593c	1
t4216c	1
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texas	1
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tree_of_life	1
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tryglycerides	1
tu	1
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turkmen	1
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type_ii_diabetes	1
tyrol	1
u2a-c	1
u2i	1
u3	1
u4	1
u6b	1
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ute	1
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uzbek	1
va	1
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vole	1
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wa	1
weiwuer	1
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women	1
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xcaret	1
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xianbei	1
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yanadi	1
yangtze	1
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yc3	1
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yorkshire	1
yoruba	1
y-qm3	1
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y_traits	1
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yukhagir	1
zang	1
zero-mode_waveguide	1
zhuangzu	1
zimbabwe	1
zuni	1

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