Kenna P - Search Results

1

Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q.

Jordan SA, Farrar GJ, Kenna P, Humphries MM, Sheils DM, Kumar-Singh R, Sharp EM, Soriano N, Ayuso C, Benitez J, et al. Jordan SA, et al. Among authors: kenna p. Nat Genet. 1993 May;4(1):54-8. doi: 10.1038/ng0593-54. Nat Genet. 1993. PMID: 8513324

2

Autosomal dominant retinitis pigmentosa (adRP): exclusion of a gene from three mapped loci provides evidence for the existence of a fourth locus.

Jordan SA, del Rio T, Soriano N, Garcia-Sandoval B, Kenna P, Ayuso C, Benitez J, Humphries P. Jordan SA, et al. Among authors: kenna p. Hum Mol Genet. 1992 Sep;1(6):411-5. doi: 10.1093/hmg/1.6.411. Hum Mol Genet. 1992. PMID: 1301915

3

Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutions.

Jordan SA, Farrar GJ, Kenna P, Humphries P. Jordan SA, et al. Among authors: kenna p. Hum Mutat. 1992;1(3):240-7. doi: 10.1002/humu.1380010311. Hum Mutat. 1992. PMID: 1301931

4

Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked family.

Farrar GJ, Findlay JB, Kumar-Singh R, Kenna P, Humphries MM, Sharpe E, Humphries P. Farrar GJ, et al. Among authors: kenna p. Hum Mol Genet. 1992 Dec;1(9):769-71. doi: 10.1093/hmg/1.9.769. Hum Mol Genet. 1992. PMID: 1302614 No abstract available.

5

Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree.

Farrar GJ, Kenna P, Jordan SA, Kumar-Singh R, Humphries MM, Sharp EM, Sheils D, Humphries P. Farrar GJ, et al. Among authors: kenna p. Genomics. 1992 Nov;14(3):805-7. doi: 10.1016/s0888-7543(05)80193-4. Genomics. 1992. PMID: 1427912

6

Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa.

Bleeker-Wagemakers LM, Gal A, Kumar-Singh R, van den Born LI, Li Y, Schwinger E, Sandkuijl LA, Bergen AA, Kenna P, Humphries P, et al. Bleeker-Wagemakers LM, et al. Among authors: kenna p. Genomics. 1992 Nov;14(3):811-2. doi: 10.1016/s0888-7543(05)80195-8. Genomics. 1992. PMID: 1427914

7

Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosa.

Horn M, Humphries P, Kunisch M, Marchese C, Apfelstedt-Sylla E, Fugi L, Zrenner E, Kenna P, Gal A, Farrar J. Horn M, et al. Among authors: kenna p. Hum Genet. 1992 Nov;90(3):255-7. doi: 10.1007/BF00220073. Hum Genet. 1992. PMID: 1487240

8

Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin.

Jordan SA, Farrar GJ, Kumar-Singh R, Kenna P, Humphries MM, Allamand V, Sharp EM, Humphries P. Jordan SA, et al. Among authors: kenna p. Am J Hum Genet. 1992 Mar;50(3):634-9. Am J Hum Genet. 1992. PMID: 1539599 Free PMC article.

9

On the molecular genetics of retinitis pigmentosa.

Humphries P, Kenna P, Farrar GJ. Humphries P, et al. Among authors: kenna p. Science. 1992 May 8;256(5058):804-8. doi: 10.1126/science.1589761. Science. 1992. PMID: 1589761 Review.

10

A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa.

Farrar GJ, Kenna P, Jordan SA, Kumar-Singh R, Humphries MM, Sharp EM, Sheils DM, Humphries P. Farrar GJ, et al. Among authors: kenna p. Nature. 1991 Dec 12;354(6353):478-80. doi: 10.1038/354478a0. Nature. 1991. PMID: 1749427

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