Genetic mapping of RP1 on 8q11-q21 in an Australian family with autosomal dominant retinitis pigmentosa reduces the critical region to 4 cM between D8S601 and D8S285

Human Genetics

Volumn 98, Issue 6, 1996, Pages 741-743

  Xu, Su Ying ^a   Denton, Michael ^b   Sullivan, Lori ^c   Daiger, Stephen P ^c   Gal, Andreas ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b UNIVERSITY OF OTAGO   (New Zealand)

^c UNIVERSITY OF TEXAS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 8Q; DOMINANT INHERITANCE; FAMILY STUDY; FEMALE; GENE MAPPING; GENETIC LINKAGE; HUMAN; MALE; MARKER GENE; PRIORITY JOURNAL; RETINITIS PIGMENTOSA;

EID: 0029909126     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050296     Document Type: Article

References (12)

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2. Blanton SH, Heckenlively JR, Cottingham JF, Sadler LA, Wagner M, Friedman LH, Daiger SP (1991) Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8. Genomics 11:857-869
3. Daiger SP, Sullivan LS, Rodriguez JA (1995) Correlation of phenotype with genotype in inherited retinal degeneration. Behav Brain Sci 18:491-506
4. Dryja TP, Li T (1995) Molecular genetics of retinitis pigmentosa. Hum Mol Genet 4:1739-1743
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8. Lehmer JM, Heckenlively JR, Stone EM, Kimura AE, Blanton SH, Daiger SP (1992) Clinical characterization of chromosome 8 autosomal dominant retinitis pigmentosa (UCLA-RP01). Invest Ophthalmol Vis Sci 33 (suppl):1396
9. Ott J (1974) Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Am J Hum Genet 26:588-617
10. Sadler LA, Blanton SH, Cottingham JF, Craft CM, Swaroop A, Wagner MJ, Heckenlively JR, Daiger SP (1991) Linkage mapping of one form of autosomal dominant retinitis pigmentosa to 8q11-q21 and exclusion of candidate genes. Am J Hum Genet 52 (suppl):A1065
11. Sullivan LS, Blanton SH, Wagner M, Heckenlively JR, Daiger SP (1995) Refined linkage and physical mapping of the chromosome 8 form of autosomal dominant retinitis pigmentosa (RP1). Cytogenet Cell Genet 68:161
12. Xu SY, Nakazawa M, Tamai M, Gal A (1995) Autosomal dominant retinitis pigmentosa locus on chromosome 19q in a Japanese family. J Med Genet 32:915-916