Literature DB >> 1762935

Dinucleotide repeat polymorphism at the human tyrosinase gene.

S W Morris1, W Muir, D St Clair.   

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Year:  1991        PMID： 1762935      PMCID： PMC329354          DOI： 10.1093/nar/19.24.6968

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  2 in total

1.  Characteristic sequences in the upstream region of the human tyrosinase gene.

Authors:  H Kikuchi; H Miura; H Yamamoto; T Takeuchi; T Dei; M Watanabe
Journal:  Biochim Biophys Acta       Date:  1989-12-22

2.  Human tyrosinase gene, mapped to chromosome 11 (q14----q21), defines second region of homology with mouse chromosome 7.

Authors:  D E Barton; B S Kwon; U Francke
Journal:  Genomics       Date:  1988-07       Impact factor: 5.736
  2 in total
  6 in total

1.  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

2.  A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico.

Authors:  W S Oetting; C J Witkop; S A Brown; R Colomer; J P Fryer; K E Bloom; R A King
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

3.  In Southern Africa, brown oculocutaneous albinism (BOCA) maps to the OCA2 locus on chromosome 15q: P-gene mutations identified.

Authors:  P Manga; J Kromberg; A Turner; T Jenkins; M Ramsay
Journal:  Am J Hum Genet       Date:  2001-02-09       Impact factor: 11.025

4.  A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2.

Authors:  S C Wildenberg; W S Oetting; C Almodóvar; M Krumwiede; J G White; R A King
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

5.  Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q.

Authors:  E C Mariman; S E van Beersum; C W Cremers; F M van Baars; H H Ropers
Journal:  Hum Genet       Date:  1993-05       Impact factor: 4.132

6.  Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources.

Authors:  J M Fletcher; K Evans; D Baillie; P Byrd; D Hanratty; S Leach; C Julier; J R Gosden; W Muir; D J Porteous
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025
  6 in total

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