Trofatter J - Search Results

1

Genetic linkage studies in autosomal dominantly inherited L-DOPA responsive parkinsonism. Evaluation of candidate genes.

Gasser T, Wszolek Z, Supala A, Trofatter J, Ozelius L, Uitti RJ, Pfeiffer RF, Gusella J, Calne D, Breakefield XO. Gasser T, et al. Among authors: trofatter j. Adv Neurol. 1996;69:87-95. Adv Neurol. 1996. PMID: 8615189 Clinical Trial. No abstract available.

2

Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes.

Gasser T, Wszolek ZK, Trofatter J, Ozelius L, Uitti RJ, Lee CS, Gusella J, Pfeiffer RF, Calne DB, Breakefield XO. Gasser T, et al. Among authors: trofatter j. Ann Neurol. 1994 Sep;36(3):387-96. doi: 10.1002/ana.410360310. Ann Neurol. 1994. PMID: 7915897

3

Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16.

Yan W, Boustany RM, Konradi C, Ozelius L, Lerner T, Trofatter JA, Julier C, Breakefield XO, Gusella JF, Haines JL. Yan W, et al. Among authors: trofatter ja. Am J Hum Genet. 1993 Jan;52(1):89-95. Am J Hum Genet. 1993. PMID: 8434611 Free PMC article.

4

Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis.

Blumenfeld A, Slaugenhaupt SA, Axelrod FB, Lucente DE, Maayan C, Liebert CB, Ozelius LJ, Trofatter JA, Haines JL, Breakefield XO, et al. Blumenfeld A, et al. Among authors: trofatter ja. Nat Genet. 1993 Jun;4(2):160-4. doi: 10.1038/ng0693-160. Nat Genet. 1993. PMID: 8102296

5

Exclusion of familial dysautonomia from more than 60% of the genome.

Blumenfeld A, Axelrod FB, Trofatter JA, Maayan C, Lucente DE, Slaugenhaupt SA, Liebert CB, Ozelius LJ, Haines JL, Breakefield XO, et al. Blumenfeld A, et al. Among authors: trofatter ja. J Med Genet. 1993 Jan;30(1):47-52. doi: 10.1136/jmg.30.1.47. J Med Genet. 1993. PMID: 8093738 Free PMC article.

6

Dinucleotide repeat polymorphism at the debrisoquine 4-hydroxylase (CYP2D) locus.

Trofatter JA, Gusella JF, Haines JL. Trofatter JA, et al. Nucleic Acids Res. 1991 May 25;19(10):2802. doi: 10.1093/nar/19.10.2802-a. Nucleic Acids Res. 1991. PMID: 2041763 Free PMC article. No abstract available.

7

An expression-independent catalog of genes from human chromosome 22.

Trofatter JA, Long KR, Murrell JR, Stotler CJ, Gusella JF, Buckler AJ. Trofatter JA, et al. Genome Res. 1995 Oct;5(3):214-24. doi: 10.1101/gr.5.3.214. Genome Res. 1995. PMID: 8593609 Free article.

8

Dinucleotide repeat polymorphism at the topoisomerase (DNA) I pseudogene 2 (TOPIP2).

Trofatter JA, Sytsma ML, Gusella JF, Haines JL. Trofatter JA, et al. Hum Mol Genet. 1992 Sep;1(6):455. doi: 10.1093/hmg/1.6.455-a. Hum Mol Genet. 1992. PMID: 1338763 No abstract available.

9

Chromosome 21 genetic linkage data set based on the Venezuelan reference pedigree.

Haines JL, Trofatter JA, Tanzi RE, Watkins P, Wexler NS, Conneally PM, Gusella JF. Haines JL, et al. Among authors: trofatter ja. Cytogenet Cell Genet. 1992;59(2-3):88-9. doi: 10.1159/000133208. Cytogenet Cell Genet. 1992. PMID: 1346592 No abstract available.

10

A genetic linkage map of the long arm of human chromosome 22.

Rouleau GA, Haines JL, Bazanowski A, Colella-Crowley A, Trofatter JA, Wexler NS, Conneally PM, Gusella JF. Rouleau GA, et al. Among authors: trofatter ja. Genomics. 1989 Jan;4(1):1-6. doi: 10.1016/0888-7543(89)90306-6. Genomics. 1989. PMID: 2563348

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