Smith DI - Search Results

1

Identification of human chromosome region 3p14.2-21.3-specific YAC clones using Alu-PCR products from a radiation hybrid.

Siden TS, Kumlien J, Drumheller T, Smith SE, Röhme D, Lehrach H, Smith DI. Siden TS, et al. Among authors: smith se, smith di. Somat Cell Mol Genet. 1994 Mar;20(2):137-42. doi: 10.1007/BF02290683. Somat Cell Mol Genet. 1994. PMID: 8009367

2

Isolation of two contigs of overlapping cosmids derived from human chromosomal band 3p21.1 and identification of 5 new 3p21.1 genes.

Shridhar V, Golembieski W, Kamat A, Smith SE, Phillips N, Miller OJ, Miller Y, Smith DI. Shridhar V, et al. Among authors: smith se, smith di. Somat Cell Mol Genet. 1994 Jul;20(4):255-65. doi: 10.1007/BF02254716. Somat Cell Mol Genet. 1994. PMID: 7974002

3

Physical map of small cell lung cancer deletion region on short arm of human chromosome 3 (3p13-22) based on radiation fusion hybrid analysis.

Siden TS, Golembieski W, Kumlien J, Röhme D, Smith DI. Siden TS, et al. Among authors: smith di. Somat Cell Mol Genet. 1994 Mar;20(2):121-32. doi: 10.1007/BF02290681. Somat Cell Mol Genet. 1994. PMID: 8009365

4

Localization of 616 human chromosome 3-specific cosmids using a somatic cell hybrid deletion mapping panel.

Smith DI, Liu W, Ginzinger D, Green P, Smith S, Wang ND, Recchia F, Carolyn K, Drabkin H, Golembieski W. Smith DI, et al. Among authors: smith s. Genomics. 1991 Sep;11(1):179-87. doi: 10.1016/0888-7543(91)90116-v. Genomics. 1991. PMID: 1662664

5

Cloning and characterization of the human t(3;6)(p14;p11) translocation breakpoint associated with hematologic malignancies.

Smith SE, Joseph A, Nadeau S, Shridhar V, Gemmill R, Drabkin H, Knuutila S, Smith DI. Smith SE, et al. Among authors: smith di. Cancer Genet Cytogenet. 1993 Nov;71(1):15-21. doi: 10.1016/0165-4608(93)90197-t. Cancer Genet Cytogenet. 1993. PMID: 8275448

6

Isolation and characterization of a 1 Mb region of 5q23.3-q31.2 surrounding the human lysyl oxidase gene.

McAlinden TP, Smith DI, Smith SE, Krawetz SA. McAlinden TP, et al. Among authors: smith se, smith di. J Mol Cell Cardiol. 1995 Oct;27(10):2409-13. doi: 10.1016/s0022-2828(95)92235-0. J Mol Cell Cardiol. 1995. PMID: 8576956

7

Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

Drumheller T, McGillivray BC, Behrner D, MacLeod P, McFadden DE, Roberson J, Venditti C, Chorney K, Chorney M, Smith DI. Drumheller T, et al. Among authors: smith di. J Med Genet. 1996 Oct;33(10):842-7. doi: 10.1136/jmg.33.10.842. J Med Genet. 1996. PMID: 8933338 Free PMC article.

8

Isolation of large numbers of chromosome 3-specific cosmids containing clusters of rare restriction-endonuclease sites.

Golembieski WA, Smith SE, Recchia F, Judge A, Shridhar V, Miller OJ, Drabkin H, Smith DI. Golembieski WA, et al. Among authors: smith se, smith di. Am J Hum Genet. 1991 Sep;49(3):581-9. Am J Hum Genet. 1991. PMID: 1652890 Free PMC article.

9

The isolation of a yeast artificial chromosome (YAC) contig extending for 2 megabases in the vicinity of the von Hippel Lindau disease gene.

Liu W, Piechocki M, Shridhar V, Lyles G, Song Z, Nakamura Y, Drabkin H, Vance J, Smith DI. Liu W, et al. Among authors: smith di. Hum Mol Genet. 1993 Aug;2(8):1177-82. doi: 10.1093/hmg/2.8.1177. Hum Mol Genet. 1993. PMID: 8104627

10

Localization of three novel hybrid breakpoints and refinement of 18 marker assignments in the human 3cen-p21.1 region.

Wang ND, Testa JR, Smith DI. Wang ND, et al. Among authors: smith di. Genomics. 1992 Dec;14(4):891-6. doi: 10.1016/s0888-7543(05)80110-7. Genomics. 1992. PMID: 1478670

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