Literature DB >> 4172140

Ocular albinism and Xg.

W G Pearce, R Sanger, R R Race.   

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Year:  1968        PMID： 4172140     DOI： 10.1016/s0140-6736(68)92295-2

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  5 in total

1.  X mapping in man: evidence against direct measurable linkage between ocular albinism and deutan colour blindness.

Authors:  W G Pearce; R Sanger
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318

2.  Abnormal crossing of the optic fibres shown by evoked magnetic fields in patients with ocular albinism with a novel mutation in the OA1 gene.

Authors:  L Lauronen; R Jalkanen; J Huttunen; E Carlsson; S Tuupanen; S Lindh; H Forsius; E-M Sankila; T Alitalo
Journal:  Br J Ophthalmol       Date:  2005-07       Impact factor: 4.638

3.  An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry.

Authors:  R E Schnur; B J Trask; G van den Engh; H H Punnett; M Kistenmacher; M A Tomeo; R E Naids; R L Nussbaum
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

4.  Nystagmus in a female carrier of ocular albinism.

Authors:  W G Pearce; G J Johnson; J G Gillan
Journal:  J Med Genet       Date:  1972-03       Impact factor: 6.318

5.  Hypoxanthine-guanine phosphoribosyltransferase deficiency and Xg blood group.

Authors:  M L Greene; W L Nyhan; J E Seegmiller
Journal:  Am J Hum Genet       Date:  1970-01       Impact factor: 11.025
  5 in total

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