Lewis RA - Search Results

1

Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacy.

Pentao L, Lewis RA, Ledbetter DH, Patel PI, Lupski JR. Pentao L, et al. Among authors: lewis ra. Am J Hum Genet. 1992 Apr;50(4):690-9. Am J Hum Genet. 1992. PMID: 1347967 Free PMC article.

2

Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.

Angel TA, Faust CJ, Gonzales JC, Kenwrick S, Lewis RA, Herman GE. Angel TA, et al. Among authors: lewis ra. Mamm Genome. 1993;4(3):171-6. doi: 10.1007/BF00352233. Mamm Genome. 1993. PMID: 8439729

3

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

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

Isolation of a candidate gene for choroideremia.

Merry DE, Jänne PA, Landers JE, Lewis RA, Nussbaum RL. Merry DE, et al. Among authors: lewis ra. Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2135-9. doi: 10.1073/pnas.89.6.2135. Proc Natl Acad Sci U S A. 1992. PMID: 1549574 Free PMC article.

6

Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.

Nussbaum RL, Lewis RA, Lesko JG, Ferrell R. Nussbaum RL, et al. Among authors: lewis ra. Am J Hum Genet. 1985 May;37(3):473-81. Am J Hum Genet. 1985. PMID: 2988333 Free PMC article.

7

Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment.

Reilly DS, Lewis RA, Ledbetter DH, Nussbaum RL. Reilly DS, et al. Among authors: lewis ra. Am J Hum Genet. 1988 May;42(5):748-55. Am J Hum Genet. 1988. PMID: 2895982 Free PMC article.

8

DXS165 detects a translocation breakpoint in a woman with choroideremia and a de novo X; 13 translocation.

Merry DE, Lesko JG, Siu V, Flintoff WF, Collins F, Lewis RA, Nussbaum RL. Merry DE, et al. Among authors: lewis ra. Genomics. 1990 Apr;6(4):609-15. doi: 10.1016/0888-7543(90)90494-f. Genomics. 1990. PMID: 2341150

9

Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.

Lesko JG, Lewis RA, Nussbaum RL. Lesko JG, et al. Among authors: lewis ra. Am J Hum Genet. 1987 Apr;40(4):303-11. Am J Hum Genet. 1987. PMID: 2883887 Free PMC article.

10

Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci.

Beales PL, Katsanis N, Lewis RA, Ansley SJ, Elcioglu N, Raza J, Woods MO, Green JS, Parfrey PS, Davidson WS, Lupski JR. Beales PL, et al. Among authors: lewis ra. Am J Hum Genet. 2001 Mar;68(3):606-16. doi: 10.1086/318794. Epub 2001 Feb 1. Am J Hum Genet. 2001. PMID: 11179009 Free PMC article.

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