Lewis RA - Search Results

1

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 Free article.

2

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.

3

Genetic and physical mapping of Xq24-q26 markers flanking the Lowe oculocerebrorenal syndrome.

Reilly DS, Lewis RA, Nussbaum RL. Reilly DS, et al. Among authors: lewis ra. Genomics. 1990 Sep;8(1):62-70. doi: 10.1016/0888-7543(90)90226-k. Genomics. 1990. PMID: 2081601 Free article.

4

Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.

Merry DE, Lesko JG, Sosnoski DM, Lewis RA, Lubinsky M, Trask B, van den Engh G, Collins FS, Nussbaum RL. Merry DE, et al. Among authors: lewis ra. Am J Hum Genet. 1989 Oct;45(4):530-40. Am J Hum Genet. 1989. PMID: 2491012 Free PMC article.

5

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.

6

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.

7

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.

8

Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation.

Nussbaum RL, Lesko JG, Lewis RA, Ledbetter SA, Ledbetter DH. Nussbaum RL, et al. Among authors: lewis ra. Proc Natl Acad Sci U S A. 1987 Sep;84(18):6521-5. doi: 10.1073/pnas.84.18.6521. Proc Natl Acad Sci U S A. 1987. PMID: 3476958 Free PMC article.

9

Mapping X-linked ophthalmic diseases. Provisional assignment of the locus for choroideremia to Xq13-q24.

Lewis RA, Nussbaum RL, Ferrell R. Lewis RA, et al. Ophthalmology. 1985 Jun;92(6):800-6. doi: 10.1016/s0161-6420(85)33956-8. Ophthalmology. 1985. PMID: 4034175

10

The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase.

Attree O, Olivos IM, Okabe I, Bailey LC, Nelson DL, Lewis RA, McInnes RR, Nussbaum RL. Attree O, et al. Among authors: lewis ra. Nature. 1992 Jul 16;358(6383):239-42. doi: 10.1038/358239a0. Nature. 1992. PMID: 1321346

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