Romano D - Search Results

1

A set of STS assays targeting the chromosome 22 physical framework markers.

MacCollin M, Romano D, Budarf M, Denny C, Trofatter J, Menon A, Rouleau G, Fontaine B, Emanuel B, Gusella J. MacCollin M, et al. Among authors: romano d. Genomics. 1993 Mar;15(3):680-3. doi: 10.1006/geno.1993.1125. Genomics. 1993. PMID: 8468063

2

Sequence-tagged sites (STSs) for a set of mapped markers on chromosome 21.

Tanzi RE, Romano DM, Berger R, Buraczynska MJ, Gaston SM, Kurnit DM, Patterson D, Gusella JF, Stewart GD. Tanzi RE, et al. Among authors: romano dm. Genomics. 1992 Oct;14(2):498-502. doi: 10.1016/s0888-7543(05)80251-4. Genomics. 1992. PMID: 1427866 Free article.

3

Increased recombination adjacent to the Huntington disease-linked D4S10 marker.

Allitto BA, MacDonald ME, Bucan M, Richards J, Romano D, Whaley WL, Falcone B, Ianazzi J, Wexler NS, Wasmuth JJ, et al. Allitto BA, et al. Among authors: romano d. Genomics. 1991 Jan;9(1):104-12. doi: 10.1016/0888-7543(91)90226-5. Genomics. 1991. PMID: 1672283 Free article.

4

A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene.

Bates GP, MacDonald ME, Baxendale S, Sedlacek Z, Youngman S, Romano D, Whaley WL, Allitto BA, Poustka A, Gusella JF, et al. Bates GP, et al. Among authors: romano d. Am J Hum Genet. 1990 Apr;46(4):762-75. Am J Hum Genet. 1990. PMID: 2138410 Free PMC article.

5

Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.

Whaley WL, Michiels F, MacDonald ME, Romano D, Zimmer M, Smith B, Leavitt J, Bucan M, Haines JL, Gilliam TC, et al. Whaley WL, et al. Among authors: romano d. Nucleic Acids Res. 1988 Dec 23;16(24):11769-80. doi: 10.1093/nar/16.24.11769. Nucleic Acids Res. 1988. PMID: 2905444 Free PMC article.

6

Mapping of cosmid clones in Huntington's disease region of chromosome 4.

Whaley WL, Bates GP, Novelletto A, Sedlacek Z, Cheng S, Romano D, Ormondroyd E, Allitto B, Lin C, Youngman S, et al. Whaley WL, et al. Among authors: romano d. Somat Cell Mol Genet. 1991 Jan;17(1):83-91. doi: 10.1007/BF01233207. Somat Cell Mol Genet. 1991. PMID: 1671801

7

Genetic heterogeneity of gene defects responsible for familial Alzheimer disease.

Tanzi R, Gaston S, Bush A, Romano D, Pettingell W, Peppercorn J, Paradis M, Gurubhagavatula S, Jenkins B, Wasco W. Tanzi R, et al. Among authors: romano d. Genetica. 1993;91(1-3):255-63. doi: 10.1007/BF01436002. Genetica. 1993. PMID: 8125274 Review.

8

Clustering of multiallele DNA markers near the Huntington's disease gene.

MacDonald ME, Cheng SV, Zimmer M, Haines JL, Poustka A, Allitto B, Smith B, Whaley WL, Romano DM, Jagadeesh J, et al. MacDonald ME, et al. Among authors: romano dm. J Clin Invest. 1989 Sep;84(3):1013-6. doi: 10.1172/JCI114222. J Clin Invest. 1989. PMID: 2569477 Free PMC article.

9

Assessment of amyloid beta-protein precursor gene mutations in a large set of familial and sporadic Alzheimer disease cases.

Tanzi RE, Vaula G, Romano DM, Mortilla M, Huang TL, Tupler RG, Wasco W, Hyman BT, Haines JL, Jenkins BJ, et al. Tanzi RE, et al. Among authors: romano dm. Am J Hum Genet. 1992 Aug;51(2):273-82. Am J Hum Genet. 1992. PMID: 1642228 Free PMC article.

10

Isolation and characterization of APLP2 encoding a homologue of the Alzheimer's associated amyloid beta protein precursor.

Wasco W, Gurubhagavatula S, Paradis MD, Romano DM, Sisodia SS, Hyman BT, Neve RL, Tanzi RE. Wasco W, et al. Among authors: romano dm. Nat Genet. 1993 Sep;5(1):95-100. doi: 10.1038/ng0993-95. Nat Genet. 1993. PMID: 8220435

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