Golembieski W - Search Results

1

A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndrome.

Gemmill RM, Varella-Garcia M, Smith DI, Erickson P, Golembieski W, Miller Y, Coyle-Morris J, Tommerup N, Drabkin HA. Gemmill RM, et al. Among authors: golembieski w. Genomics. 1991 Sep;11(1):93-102. doi: 10.1016/0888-7543(91)90105-n. Genomics. 1991. PMID: 1662666

2

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: golembieski w. Genomics. 1991 Sep;11(1):179-87. doi: 10.1016/0888-7543(91)90116-v. Genomics. 1991. PMID: 1662664

3

Saturation of human chromosome 3 with unique sequence hybridization probes.

Smith DI, Mangrulker R, Geist R, Gilbert J, Kinsman K, Drabkin H, Golembieski W. Smith DI, et al. Among authors: golembieski w. Genomics. 1989 May;4(4):453-9. doi: 10.1016/0888-7543(89)90268-1. Genomics. 1989. PMID: 2744758

4

Identification of two cosmids derived from within chromosomal band 3p21.1 that contain clusters of rare restriction sites and evolutionarily conserved sequences.

Smith DI, Golembieski W, Drabkin H, Kiousis S. Smith DI, et al. Among authors: golembieski w. Am J Hum Genet. 1989 Sep;45(3):443-7. Am J Hum Genet. 1989. PMID: 2570530 Free PMC article.

5

Mapping of the gene for human cysteine proteinase inhibitor stefin A, STF1, to chromosome 3cen-q21.

Hsieh WT, Fong D, Sloane BF, Golembieski W, Smith DI. Hsieh WT, et al. Among authors: golembieski w. Genomics. 1991 Jan;9(1):207-9. doi: 10.1016/0888-7543(91)90241-6. Genomics. 1991. PMID: 2004763

6

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: golembieski w. Somat Cell Mol Genet. 1994 Jul;20(4):255-65. doi: 10.1007/BF02254716. Somat Cell Mol Genet. 1994. PMID: 7974002

7

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: golembieski w. Somat Cell Mol Genet. 1994 Mar;20(2):121-32. doi: 10.1007/BF02290681. Somat Cell Mol Genet. 1994. PMID: 8009365

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. Am J Hum Genet. 1991 Sep;49(3):581-9. Am J Hum Genet. 1991. PMID: 1652890 Free PMC article.

9

A StuI polymorphism on chromosome 3p14.1-14.2 (D3S622) defined by two polymorphic StuI sites 2.4 kb apart.

Secore SL, Walker AP, Herbstreith MH, Siddique T, Jeffers AJ, DeShields TR, Speer MC, Pericak-Vance MA, Golembieski WA, Smith DI, et al. Secore SL, et al. Among authors: golembieski wa. Nucleic Acids Res. 1991 Nov 25;19(22):6349. doi: 10.1093/nar/19.22.6349. Nucleic Acids Res. 1991. PMID: 1956809 Free PMC article. No abstract available.

10

Overabundance of rare-cutting restriction endonuclease sites in the human genome.

Smith DI, Golembieski W, Gilbert JD, Kizyma L, Miller OJ. Smith DI, et al. Among authors: golembieski w. Nucleic Acids Res. 1987 Feb 11;15(3):1173-84. doi: 10.1093/nar/15.3.1173. Nucleic Acids Res. 1987. PMID: 3029699 Free PMC article.

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