Sparkes RS - Search Results

1

Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract.

Geyer DD, Spence MA, Johannes M, Flodman P, Clancy KP, Berry R, Sparkes RS, Jonsen MD, Isenberg SJ, Bateman JB. Geyer DD, et al. Among authors: sparkes rs. Am J Ophthalmol. 2006 Apr;141(4):761-3. doi: 10.1016/j.ajo.2005.11.008. Am J Ophthalmol. 2006. PMID: 16564824 Free PMC article.

2

Genetic linkage analysis of autosomal dominant congenital cataracts with lens-specific DNA probes and polymorphic phenotypic markers.

Barrett DJ, Sparkes RS, Gorin MB, Bhat SP, Spence MA, Marazita ML, Bateman JB. Barrett DJ, et al. Among authors: sparkes rs. Ophthalmology. 1988 Apr;95(4):538-44. doi: 10.1016/s0161-6420(88)33153-2. Ophthalmology. 1988. PMID: 3174013

3

Genetic linkage analysis of autosomal dominant congenital cataracts.

Bateman JB, Spence MA, Marazita ML, Sparkes RS. Bateman JB, et al. Among authors: sparkes rs. Am J Ophthalmol. 1986 Feb 15;101(2):218-25. doi: 10.1016/0002-9394(86)90599-4. Am J Ophthalmol. 1986. PMID: 3456204

4

A new locus for autosomal dominant cataract on chromosome 12q13.

Bateman JB, Johannes M, Flodman P, Geyer DD, Clancy KP, Heinzmann C, Kojis T, Berry R, Sparkes RS, Spence MA. Bateman JB, et al. Among authors: sparkes rs. Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2665-70. Invest Ophthalmol Vis Sci. 2000. PMID: 10937580

5

Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa.

Kojis TL, Heinzmann C, Flodman P, Ngo JT, Sparkes RS, Spence MA, Bateman JB, Heckenlively JR. Kojis TL, et al. Among authors: sparkes rs. Am J Hum Genet. 1996 Feb;58(2):347-55. Am J Hum Genet. 1996. PMID: 8571961 Free PMC article.

6

Recombinational event between Norrie disease and DXS7 loci.

Ngo JT, Spence MA, Cortessis V, Sparkes RS, Bateman JB. Ngo JT, et al. Among authors: sparkes rs. Clin Genet. 1988 Jul;34(1):43-7. doi: 10.1111/j.1399-0004.1988.tb02614.x. Clin Genet. 1988. PMID: 2900708

7

The gene for the major intrinsic protein (MIP) of the ocular lens is assigned to human chromosome 12cen-q14.

Sparkes RS, Mohandas T, Heinzmann C, Gorin MB, Horwitz J, Law ML, Jones CA, Bateman JB. Sparkes RS, et al. Invest Ophthalmol Vis Sci. 1986 Sep;27(9):1351-4. Invest Ophthalmol Vis Sci. 1986. PMID: 3017887

8

The Rieger syndrome and a chromosome 13 deletion.

Stathacopoulos RA, Bateman JB, Sparkes RS, Hepler RS. Stathacopoulos RA, et al. Among authors: sparkes rs. J Pediatr Ophthalmol Strabismus. 1987 Jul-Aug;24(4):198-203. doi: 10.3928/0191-3913-19870701-12. J Pediatr Ophthalmol Strabismus. 1987. PMID: 3117999

9

Peters' anomaly associated with partial deletion of the long arm of chromosome 11.

Bateman JB, Maumenee IH, Sparkes RS. Bateman JB, et al. Among authors: sparkes rs. Am J Ophthalmol. 1984 Jan;97(1):11-5. doi: 10.1016/0002-9394(84)90440-9. Am J Ophthalmol. 1984. PMID: 6696011

10

Regional mapping of the human MP70 (Cx50; connexin 50) gene by fluorescence in situ hybridization to 1q21.1.

Geyer DD, Church RL, Steele EC Jr, Heinzmann C, Kojis TL, Klisak I, Sparkes RS, Bateman JB. Geyer DD, et al. Among authors: sparkes rs. Mol Vis. 1997 Dec 17;3:13. Mol Vis. 1997. PMID: 9479004 Free article.

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