Cavenee W - Search Results

1

A primary genetic map of chromosome 13q.

Leppert M, Cavenee W, Callahan P, Holm T, O'Connell P, Thompson K, Lathrop GM, Lalouel JM, White R. Leppert M, et al. Among authors: cavenee w. Am J Hum Genet. 1986 Oct;39(4):425-37. Am J Hum Genet. 1986. PMID: 3464200 Free PMC article.

2

Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.

Cavenee W, Leach R, Mohandas T, Pearson P, White R. Cavenee W, et al. Am J Hum Genet. 1984 Jan;36(1):10-24. Am J Hum Genet. 1984. PMID: 6320640 Free PMC article.

3

A genetic linkage map with 29 loci spanning human chromosome 13q.

Gerken S, Leppert M, O'Connell P, Cavenee W, James CD, Ballard L, Stauffer D, Elsner T, Plaetke R, Lalouel JM, et al. Gerken S, et al. Among authors: cavenee w. Genomics. 1993 May;16(2):515-9. doi: 10.1006/geno.1993.1219. Genomics. 1993. PMID: 8100218

4

The genetic basis of cancer.

Cavenee WK, White RL. Cavenee WK, et al. Sci Am. 1995 Mar;272(3):72-9. doi: 10.1038/scientificamerican0395-72. Sci Am. 1995. PMID: 7871410 Review. No abstract available.

5

Homozygosity of chromosome 13 in retinoblastoma.

Dryja TP, Cavenee W, White R, Rapaport JM, Petersen R, Albert DM, Bruns GA. Dryja TP, et al. Among authors: cavenee w. N Engl J Med. 1984 Mar 1;310(9):550-3. doi: 10.1056/NEJM198403013100902. N Engl J Med. 1984. PMID: 6694706

6

Chromosome 13 homozygosity in osteosarcoma without retinoblastoma.

Dryja TP, Rapaport JM, Epstein J, Goorin AM, Weichselbaum R, Koufos A, Cavenee WK. Dryja TP, et al. Among authors: cavenee wk. Am J Hum Genet. 1986 Jan;38(1):59-66. Am J Hum Genet. 1986. PMID: 3004203 Free PMC article.

7

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma.

Cavenee WK, Dryja TP, Phillips RA, Benedict WF, Godbout R, Gallie BL, Murphree AL, Strong LC, White RL. Cavenee WK, et al. Nature. 1983 Oct 27-Nov 2;305(5937):779-84. doi: 10.1038/305779a0. Nature. 1983. PMID: 6633649

8

Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10.

Karlbom AE, James CD, Boethius J, Cavenee WK, Collins VP, Nordenskjöld M, Larsson C. Karlbom AE, et al. Among authors: cavenee wk. Hum Genet. 1993 Sep;92(2):169-74. doi: 10.1007/BF00219686. Hum Genet. 1993. PMID: 8370584

9

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

Koufos A, Grundy P, Morgan K, Aleck KA, Hadro T, Lampkin BC, Kalbakji A, Cavenee WK. Koufos A, et al. Among authors: cavenee wk. Am J Hum Genet. 1989 May;44(5):711-9. Am J Hum Genet. 1989. PMID: 2539717 Free PMC article.

10

A new highly polymorphic DNA restriction site marker in the 5' region of the human tyrosine hydroxylase gene (TH) detecting loss of heterozygosity in human embryonal rhabdomyosarcoma.

Besnard-Guérin C, Cavenee WK, Newsham I. Besnard-Guérin C, et al. Among authors: cavenee wk. Hum Genet. 1994 Mar;93(3):349-50. doi: 10.1007/BF00212038. Hum Genet. 1994. PMID: 7510263

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