Schellenberg GD - Search Results

1

Dinucleotide repeat polymorphisms at the GSR gene.

Yu CE, Anderson L, Oshima J, Schellenberg GD. Yu CE, et al. Among authors: schellenberg gd. Hum Mol Genet. 1994 Jan;3(1):212. Hum Mol Genet. 1994. PMID: 8162038 No abstract available.

2

Dinucleotide repeat polymorphism at the D14S294 locus.

Fu CW, Anderson L, Schellenberg G. Fu CW, et al. Hum Mol Genet. 1993 Oct;2(10):1751. doi: 10.1093/hmg/2.10.1751-a. Hum Mol Genet. 1993. PMID: 8268948 No abstract available.

3

Dinucleotide repeat polymorphism at the D8S131 locus.

Yu CE, Anderson L, Oshima J, Schellenberg GD. Yu CE, et al. Among authors: schellenberg gd. Hum Mol Genet. 1994 Jan;3(1):211. Hum Mol Genet. 1994. PMID: 8162035 No abstract available.

4

Dinucleotide repeat polymorphism at the FGFR1 gene.

Yu CE, Anderson L, Oshima J, Schellenberg GD. Yu CE, et al. Among authors: schellenberg gd. Hum Mol Genet. 1994 Jan;3(1):212. Hum Mol Genet. 1994. PMID: 8162037 No abstract available.

5

Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.

Goddard KA, Yu CE, Oshima J, Miki T, Nakura J, Piussan C, Martin GM, Schellenberg GD, Wijsman EM. Goddard KA, et al. Among authors: schellenberg gd. Am J Hum Genet. 1996 Jun;58(6):1286-302. Am J Hum Genet. 1996. PMID: 8651307 Free PMC article.

6

APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.

Schellenberg GD, Anderson L, O'dahl S, Wisjman EM, Sadovnick AD, Ball MJ, Larson EB, Kukull WA, Martin GM, Roses AD, et al. Schellenberg GD, et al. Am J Hum Genet. 1991 Sep;49(3):511-7. Am J Hum Genet. 1991. PMID: 1679288 Free PMC article.

7

Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.

Schellenberg GD, Pericak-Vance MA, Wijsman EM, Moore DK, Gaskell PC Jr, Yamaoka LA, Bebout JL, Anderson L, Welsh KA, Clark CM, et al. Schellenberg GD, et al. Am J Hum Genet. 1991 Mar;48(3):563-83. Am J Hum Genet. 1991. PMID: 1998342 Free PMC article.

8

Cloning, sequencing, and mapping of the human chromosome 14 heat shock protein gene (HSPA2).

Bonnycastle LL, Yu CE, Hunt CR, Trask BJ, Clancy KP, Weber JL, Patterson D, Schellenberg GD. Bonnycastle LL, et al. Among authors: schellenberg gd. Genomics. 1994 Sep 1;23(1):85-93. doi: 10.1006/geno.1994.1462. Genomics. 1994. PMID: 7829106

9

Chromosome 14 and late-onset familial Alzheimer disease (FAD).

Schellenberg GD, Payami H, Wijsman EM, Orr HT, Goddard KA, Anderson L, Nemens E, White JA, Alonso ME, Ball MJ, et al. Schellenberg GD, et al. Am J Hum Genet. 1993 Sep;53(3):619-28. Am J Hum Genet. 1993. PMID: 8352272 Free PMC article.

10

Positional cloning of the Werner's syndrome gene.

Yu CE, Oshima J, Fu YH, Wijsman EM, Hisama F, Alisch R, Matthews S, Nakura J, Miki T, Ouais S, Martin GM, Mulligan J, Schellenberg GD. Yu CE, et al. Among authors: schellenberg gd. Science. 1996 Apr 12;272(5259):258-62. doi: 10.1126/science.272.5259.258. Science. 1996. PMID: 8602509

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