PubMed

Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness.

Kenna P, Mansergh F, Millington-Ward S, Erven A, Kumar-Singh R, Brennan R, Farrar GJ, Humphries P.

Br J Ophthalmol. 1997 Mar;81(3):207-13.PMID: 9135384 [PubMed - indexed for MEDLINE]Related articlesFree article

Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6.

Farrar GJ, Jordan SA, Kenna P, Humphries MM, Kumar-Singh R, McWilliam P, Allamand V, Sharp E, Humphries P.

Genomics. 1991 Dec;11(4):870-4. Erratum in: Genomics 1992 Aug;13(4):1384. PMID: 1783395 [PubMed - indexed for MEDLINE]Related articles

An autosomal dominant retinitis pigmentosa family with close linkage to D7S480 on 7q.

Millán JM, Martínez F, Vilela C, Beneyto M, Prieto F, Nájera C.

Hum Genet. 1995 Aug;96(2):216-8.PMID: 7635473 [PubMed - indexed for MEDLINE]Related articles

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.

Nat Genet. 1993 May;4(1):54-8.PMID: 8513324 [PubMed - indexed for MEDLINE]Related articles

An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q.

Bardien S, Ebenezer N, Greenberg J, Inglehearn CF, Bartmann L, Goliath R, Beighton P, Ramesar R, Bhattacharya SS.

Hum Mol Genet. 1995 Aug;4(8):1459-62.PMID: 7581389 [PubMed - indexed for MEDLINE]Related articles

Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family.

McGuire RE, Gannon AM, Sullivan LS, Rodriguez JA, Daiger SP.

Hum Genet. 1995 Jan;95(1):71-4.PMID: 7814030 [PubMed - indexed for MEDLINE]Related articles

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.

Hum Mol Genet. 1992 Sep;1(6):411-5.PMID: 1301915 [PubMed - indexed for MEDLINE]Related articles

Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family.

Kumar A, Shetty J, Kumar B, Blanton SH.

Mol Vis. 2004 Jun 15;10:399-402.PMID: 15215745 [PubMed - indexed for MEDLINE]Related articlesFree article

Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.

Zhang Q, Zulfiqar F, Riazuddin SA, Xiao X, Ahmad Z, Riazuddin S, Hejtmancik JF.

Mol Vis. 2004 Nov 17;10:884-9.PMID: 15570217 [PubMed - indexed for MEDLINE]Related articlesFree article

Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3.

Olsson JE, Samanns C, Jimenez J, Pongratz J, Chand A, Watty A, Seuchter SA, Denton M, Gal A.

Am J Med Genet. 1990 Apr;35(4):595-9.PMID: 2333895 [PubMed - indexed for MEDLINE]Related articles

A novel locus (RP33) for autosomal dominant retinitis pigmentosa mapping to chromosomal region 2cen-q12.1.

Zhao C, Lu S, Zhou X, Zhang X, Zhao K, Larsson C.

Hum Genet. 2006 Jul;119(6):617-23. Epub 2006 Apr 13.PMID: 16612614 [PubMed - indexed for MEDLINE]Related articles

[A study on localization of an autosomal dominant retinitis pigmentosa gene]

Ma X, Wei R, Cai J, Zhu L.

Zhonghua Yan Ke Za Zhi. 2002 Nov;38(11):680-3. Chinese. PMID: 12487900 [PubMed - indexed for MEDLINE]Related articles

Autosomal dominant retinitis pigmentosa locus on chromosome 19q in a Japanese family.

Xu S, Nakazawa M, Tamai M, Gal A.

J Med Genet. 1995 Nov;32(11):915-6.PMID: 8592343 [PubMed - indexed for MEDLINE]Related articlesFree article

Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY2): evidence of an RP locus on chromosome 1.

Spence MA, Sparkes RS, Heckenlively JR, Pearlman JT, Zedalis D, Sparkes M, Crist M, Tideman S.

Am J Hum Genet. 1977 Jul;29(4):397-404.PMID: 879170 [PubMed - indexed for MEDLINE]Related articlesFree article

Association of a novel mutation in the retinol dehydrogenase 12 (RDH12) gene with autosomal dominant retinitis pigmentosa.

Fingert JH, Oh K, Chung M, Scheetz TE, Andorf JL, Johnson RM, Sheffield VC, Stone EM.

Arch Ophthalmol. 2008 Sep;126(9):1301-7.PMID: 18779497 [PubMed - indexed for MEDLINE]Related articlesFree article

Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3.

McWilliam P, Farrar GJ, Kenna P, Bradley DG, Humphries MM, Sharp EM, McConnell DJ, Lawler M, Sheils D, Ryan C, et al.

Genomics. 1989 Oct;5(3):619-22.PMID: 2613244 [PubMed - indexed for MEDLINE]Related articles

Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease.

Humphries P, Farrar GJ, Kenna P, McWilliam P.

Clin Genet. 1990 Jul;38(1):1-13. Review.PMID: 2201466 [PubMed - indexed for MEDLINE]Related articles

Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.

Prakash S, Chung KW, Sinha S, Barmada M, Ellis D, Ferrell RE, Finegold DN, Randhawa PS, Dinda A, Vats A.

J Am Soc Nephrol. 2003 Jul;14(7):1794-803.PMID: 12819239 [PubMed - indexed for MEDLINE]Related articlesFree article

[Exclusive gene mapping on retinitis pigmentosa with markers on chromosomes 3 in a Chinese kindred]

Liu Z, Deng H, Xi XH, Xia JH, Pan Q, Dai HP, Yang YJ, Deng HX, Xia K, Zheng D.

Zhonghua Yan Ke Za Zhi. 2003 Apr;39(4):206-8. Chinese. PMID: 12882697 [PubMed - indexed for MEDLINE]Related articles

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, Friedman LH, Daiger SP.

Genomics. 1991 Dec;11(4):857-69.PMID: 1783394 [PubMed - indexed for MEDLINE]Related articles