Kostrzewa M - Search Results

1

Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome.

Jaju RJ, Boultwood J, Oliver FJ, Kostrzewa M, Fidler C, Parker N, McPherson JD, Morris SW, Müller U, Wainscoat JS, Kearney L. Jaju RJ, et al. Among authors: kostrzewa m. Genes Chromosomes Cancer. 1998 Jul;22(3):251-6. doi: 10.1002/(sici)1098-2264(199807)22:3<251::aid-gcc11>3.0.co;2-r. Genes Chromosomes Cancer. 1998. PMID: 9624537

2

Novel genes mapping to the critical region of the 5q- syndrome.

Boultwood J, Fidler C, Soularue P, Strickson AJ, Kostrzewa M, Jaju RJ, Cotter FE, Fairweather N, Monaco AP, Müller U, Lovett M, Jabs EW, Auffray C, Wainscoat JS. Boultwood J, et al. Among authors: kostrzewa m. Genomics. 1997 Oct 1;45(1):88-96. doi: 10.1006/geno.1997.4899. Genomics. 1997. PMID: 9339364 Free article.

3

Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs.

Boultwood J, Fidler C, Strickson AJ, Watkins F, Kostrzewa M, Jaju RJ, Müller U, Wainscoat JS. Boultwood J, et al. Among authors: kostrzewa m. Genomics. 2000 May 15;66(1):26-34. doi: 10.1006/geno.2000.6193. Genomics. 2000. PMID: 10843801

4

Transcript map of the chromosome 2-linked autosomal dominant spastic paraplegia (SPG4) critical region and identification of a highly informative STRP.

Lau EL, Kostrzewa M, Müller U. Lau EL, et al. Among authors: kostrzewa m. Neurogenetics. 1998 Dec;2(1):75-6. doi: 10.1007/s100480050055. Neurogenetics. 1998. PMID: 9933304 No abstract available.

5

Genomic structure and complete sequence of the human FGFR4 gene.

Kostrzewa M, Müller U. Kostrzewa M, et al. Mamm Genome. 1998 Feb;9(2):131-5. doi: 10.1007/s003359900703. Mamm Genome. 1998. PMID: 9457674

6

Integration of four genes, a pseudogene, thirty-one STSs, and a highly polymorphic STRP into the 7-10 Mb YAC contig of 5q34-q35.

Kostrzewa M, Grady DL, Moyzis RK, Flöter L, Müller U. Kostrzewa M, et al. Hum Genet. 1996 Mar;97(3):399-403. doi: 10.1007/BF02185781. Hum Genet. 1996. PMID: 8786091

7

Assignment of genes encoding GABAA receptor subunits alpha 1, alpha 6, beta 2, and gamma 2 to a YAC contig of 5q33.

Kostrzewa M, Köhler A, Eppelt K, Hellam L, Fairweather ND, Levy ER, Monaco AP, Müller U. Kostrzewa M, et al. Eur J Hum Genet. 1996;4(4):199-204. doi: 10.1159/000472199. Eur J Hum Genet. 1996. PMID: 8875185

8

Locus heterogeneity in Friedreich ataxia.

Kostrzewa M, Klockgether T, Damian MS, Müller U. Kostrzewa M, et al. Neurogenetics. 1997 May;1(1):43-7. doi: 10.1007/s100480050007. Neurogenetics. 1997. PMID: 10735274

9

Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3).

Németh AH, Nolte D, Dunne E, Niemann S, Kostrzewa M, Peters U, Fraser E, Bochukova E, Butler R, Brown J, Cox RD, Levy ER, Ropers HH, Monaco AP, Müller U. Németh AH, et al. Among authors: kostrzewa m. Genomics. 1999 Sep 15;60(3):320-9. doi: 10.1006/geno.1999.5929. Genomics. 1999. PMID: 10493831

10

Genomic mapping and evolution of human GABA(A) receptor subunit gene clusters.

Bailey ME, Matthews DA, Riley BP, Albrecht BE, Kostrzewa M, Hicks AA, Harris R, Müller U, Darlison MG, Johnson KJ. Bailey ME, et al. Among authors: kostrzewa m. Mamm Genome. 1999 Aug;10(8):839-43. doi: 10.1007/s003359901101. Mamm Genome. 1999. PMID: 10430673 No abstract available.

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