Denton MJ - Search Results

1

Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan.

Leutelt J, Oehlmann R, Younus F, van den Born LI, Weber JL, Denton MJ, Mehdi SQ, Gal A. Leutelt J, et al. Among authors: denton mj. Clin Genet. 1995 Mar;47(3):122-4. doi: 10.1111/j.1399-0004.1995.tb03943.x. Clin Genet. 1995. PMID: 7634534

2

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.

Xu SY, Denton M, Sullivan L, Daiger SP, Gal A. Xu SY, et al. Hum Genet. 1996 Dec;98(6):741-3. doi: 10.1007/s004390050296. Hum Genet. 1996. PMID: 8931712

3

Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3.

Finckh U, Xu S, Kumaramanickavel G, Schürmann M, Mukkadan JK, Fernandez ST, John S, Weber JL, Denton MJ, Gal A. Finckh U, et al. Among authors: denton mj. Genomics. 1998 Mar 15;48(3):341-5. doi: 10.1006/geno.1997.5194. Genomics. 1998. PMID: 9545639

4

Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian family.

Gu S, Kumaramanickavel G, Srikumari CR, Denton MJ, Gal A. Gu S, et al. Among authors: denton mj. J Med Genet. 1999 Sep;36(9):705-7. J Med Genet. 1999. PMID: 10507729 Free PMC article.

5

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. Olsson JE, et al. Am J Med Genet. 1990 Apr;35(4):595-9. doi: 10.1002/ajmg.1320350434. Am J Med Genet. 1990. PMID: 2333895

6

Evidence against a second autosomal dominant retinitis pigmentosa locus close to rhodopsin on chromosome 3q.

Inglehearn C, Farrar J, Denton M, Gal A, Humphries P, Bhattacharya S. Inglehearn C, et al. Am J Hum Genet. 1993 Aug;53(2):536-7. Am J Hum Genet. 1993. PMID: 8328469 Free PMC article. No abstract available.

7

Two different genes for X-linked retinitis pigmentosa.

Wirth B, Denton MJ, Chen JD, Neugebauer M, Halliday FB, van Schooneveld M, Donald J, Bleeker-Wagemakers EM, Pearson PL, Gal A. Wirth B, et al. Among authors: denton mj. Genomics. 1988 Apr;2(3):263-6. doi: 10.1016/0888-7543(88)90011-0. Genomics. 1988. PMID: 3397063

8

Oguchi disease: suggestion of linkage to markers on chromosome 2q.

Maw MA, John S, Jablonka S, Müller B, Kumaramanickavel G, Oehlmann R, Denton MJ, Gal A. Maw MA, et al. Among authors: denton mj. J Med Genet. 1995 May;32(5):396-8. doi: 10.1136/jmg.32.5.396. J Med Genet. 1995. PMID: 7616550 Free PMC article.

9

Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosa.

Fuchs S, Kranich H, Denton MJ, Zrenner E, Bhattacharya SS, Humphries P, Gal A. Fuchs S, et al. Among authors: denton mj. Hum Mol Genet. 1994 Jul;3(7):1203. doi: 10.1093/hmg/3.7.1203. Hum Mol Genet. 1994. PMID: 7981701 No abstract available.

10

Missense rhodopsin mutation in a family with recessive RP.

Kumaramanickavel G, Maw M, Denton MJ, John S, Srikumari CR, Orth U, Oehlmann R, Gal A. Kumaramanickavel G, et al. Among authors: denton mj. Nat Genet. 1994 Sep;8(1):10-1. doi: 10.1038/ng0994-10. Nat Genet. 1994. PMID: 7987385 No abstract available.

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