Lewis RA - Search Results

1

Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium.

Smith RJ, Berlin CI, Hejtmancik JF, Keats BJ, Kimberling WJ, Lewis RA, Möller CG, Pelias MZ, Tranebjaerg L. Smith RJ, et al. Among authors: lewis ra. Am J Med Genet. 1994 Mar 1;50(1):32-8. doi: 10.1002/ajmg.1320500107. Am J Med Genet. 1994. PMID: 8160750

2

Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium.

Keats BJ, Todorov AA, Atwood LD, Pelias MZ, Hejtmancik JF, Kimberling WJ, Leppert M, Lewis RA, Smith RJ. Keats BJ, et al. Among authors: lewis ra. Genomics. 1992 Nov;14(3):707-14. doi: 10.1016/s0888-7543(05)80172-7. Genomics. 1992. PMID: 1427898

3

DNA linkage studies of degenerative retinal diseases.

Daiger SP, Heckenlively JR, Lewis RA, Pelias MZ. Daiger SP, et al. Among authors: lewis ra. Prog Clin Biol Res. 1987;247:147-62. Prog Clin Biol Res. 1987. PMID: 3317443 Review.

4

Mapping X-linked ophthalmic diseases. III. Provisional assignment of the locus for blue cone monochromacy to Xq28.

Lewis RA, Holcomb JD, Bromley WC, Wilson MC, Roderick TH, Hejtmancik JF. Lewis RA, et al. Arch Ophthalmol. 1987 Aug;105(8):1055-9. doi: 10.1001/archopht.1987.01060080057028. Arch Ophthalmol. 1987. PMID: 2888453

5

Molecular genetics of human blue cone monochromacy.

Nathans J, Davenport CM, Maumenee IH, Lewis RA, Hejtmancik JF, Litt M, Lovrien E, Weleber R, Bachynski B, Zwas F, et al. Nathans J, et al. Among authors: lewis ra. Science. 1989 Aug 25;245(4920):831-8. doi: 10.1126/science.2788922. Science. 1989. PMID: 2788922

6

Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients.

Wang LL, Levy ML, Lewis RA, Chintagumpala MM, Lev D, Rogers M, Plon SE. Wang LL, et al. Among authors: lewis ra. Am J Med Genet. 2001 Jul 22;102(1):11-7. doi: 10.1002/1096-8628(20010722)102:1<11::aid-ajmg1413>3.0.co;2-a. Am J Med Genet. 2001. PMID: 11471165

7

Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2).

Greenberg F, Lewis RA, Potocki L, Glaze D, Parke J, Killian J, Murphy MA, Williamson D, Brown F, Dutton R, McCluggage C, Friedman E, Sulek M, Lupski JR. Greenberg F, et al. Among authors: lewis ra. Am J Med Genet. 1996 Mar 29;62(3):247-54. doi: 10.1002/(SICI)1096-8628(19960329)62:3<247::AID-AJMG9>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8882782

8

Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.

Lewis RA, Otterud B, Stauffer D, Lalouel JM, Leppert M. Lewis RA, et al. Genomics. 1990 Jun;7(2):250-6. doi: 10.1016/0888-7543(90)90547-8. Genomics. 1990. PMID: 1971808

9

Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.

Leppert M, Baird L, Anderson KL, Otterud B, Lupski JR, Lewis RA. Leppert M, et al. Among authors: lewis ra. Nat Genet. 1994 May;7(1):108-12. doi: 10.1038/ng0594-108. Nat Genet. 1994. PMID: 8075632

10

A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epithelium.

Lyons LA, Lewis RA, Strong LC, Zuckerbrod S, Ferrell RE. Lyons LA, et al. Among authors: lewis ra. Am J Hum Genet. 1988 Feb;42(2):290-6. Am J Hum Genet. 1988. PMID: 3422541 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,073 results

Search Page