Literature DB >> 5579410

A distinctive pigment of the skin in New Guinea indigenes.

R J Walsh.   

Abstract

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Year:  1971        PMID： 5579410     DOI： 10.1111/j.1469-1809.1971.tb00250.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


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  5 in total

1.  The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.

Authors:  M Ramsay; M A Colman; G Stevens; E Zwane; J Kromberg; M Farrall; T Jenkins
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

2.  Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene.

Authors:  P Manga; J G Kromberg; N F Box; R A Sturm; T Jenkins; M Ramsay
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

Review 3.  Human skin pigmentation, its genetics and variations.

Authors:  A K Kalla
Journal:  Humangenetik       Date:  1974-03-28

4.  Congenital nystagmus among the Red-skins of the Highlands of Papua New Guinea.

Authors:  R W Hornabrook; W I McDonald; R L Carroll
Journal:  Br J Ophthalmol       Date:  1980-05       Impact factor: 4.638

5.  An intragenic deletion of the P gene is the common mutation causing tyrosinase-positive oculocutaneous albinism in southern African Negroids.

Authors:  G Stevens; J van Beukering; T Jenkins; M Ramsay
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025
  5 in total

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