Lesko JG - 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: lesko jg. Genomics. 1990 Apr;6(4):609-15. doi: 10.1016/0888-7543(90)90494-f. Genomics. 1990. PMID: 2341150 Free article.

2

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: lesko jg. Am J Hum Genet. 1989 Oct;45(4):530-40. Am J Hum Genet. 1989. PMID: 2491012 Free PMC article.

3

Linkage studies and deletion screening in choroideremia.

Wright AF, Nussbaum RL, Bhattacharya SS, Jay M, Lesko JG, Evans HJ, Jay B. Wright AF, et al. Among authors: lesko jg. J Med Genet. 1990 Aug;27(8):496-8. doi: 10.1136/jmg.27.8.496. J Med Genet. 1990. PMID: 1976814 Free PMC article.

4

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. Am J Hum Genet. 1987 Apr;40(4):303-11. Am J Hum Genet. 1987. PMID: 2883887 Free PMC article.

5

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: lesko jg. Am J Hum Genet. 1985 May;37(3):473-81. Am J Hum Genet. 1985. PMID: 2988333 Free PMC article.

6

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: lesko jg. 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.

7

Linkage analysis of a large Latin-American family with X-linked retinitis pigmentosa and metallic sheen in the heterozygote carrier.

Musarella MA, Anson-Cartwright L, Burghes A, Worton RG, Lesko JG, Nussbaum RL. Musarella MA, et al. Among authors: lesko jg. Genomics. 1989 May;4(4):601-5. doi: 10.1016/0888-7543(89)90285-1. Genomics. 1989. PMID: 2568332

8

RFLP locus DXS42 is proximal to the locus for hypoxanthine phosphoribosyltransferase.

Lesko JG, Nussbaum RL. Lesko JG, et al. Am J Hum Genet. 1986 Nov;39(5):669-70. Am J Hum Genet. 1986. PMID: 2878611 Free PMC article. No abstract available.

9

Thymidylate synthase-deficient Chinese hamster cells: a selection system for human chromosome 18 and experimental system for the study of thymidylate synthase regulation and fragile X expression.

Nussbaum RL, Walmsley RM, Lesko JG, Airhart SD, Ledbetter DH. Nussbaum RL, et al. Among authors: lesko jg. Am J Hum Genet. 1985 Nov;37(6):1192-205. Am J Hum Genet. 1985. PMID: 3002173 Free PMC article.

10

Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers.

Nussbaum RL, Lewis RA, Lesko JG, Ferrell R. Nussbaum RL, et al. Among authors: lesko jg. Hum Genet. 1985;70(1):45-50. doi: 10.1007/BF00389458. Hum Genet. 1985. PMID: 3858218

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