Senger G - Search Results

1

Microdissection of chromosome band 11p15.5: characterization of probes mapping distal to the HBBC locus.

Newsham I, Claussen U, Lüdecke HJ, Mason M, Senger G, Horsthemke B, Cavenee W. Newsham I, et al. Among authors: senger g. Genes Chromosomes Cancer. 1991 Mar;3(2):108-16. doi: 10.1002/gcc.2870030205. Genes Chromosomes Cancer. 1991. PMID: 1676905

2

Characterization of a microdissection library from human chromosome region 3p14.

Bardenheuer W, Szymanski S, Lux A, Lüdecke HJ, Horsthemke B, Claussen U, Senger G, Smith DI, Wang ND, LePaslier D, et al. Bardenheuer W, et al. Among authors: senger g. Genomics. 1994 Jan 15;19(2):291-7. doi: 10.1006/geno.1994.1060. Genomics. 1994. PMID: 8188259

3

Characterization and mapping of microdissected genomic clones from the adenomatous polyposis coli (APC) region.

Hampton G, Leuteritz G, Lüdecke HJ, Senger G, Trautmann U, Thomas H, Solomon E, Bodmer WF, Horsthemke B, Claussen U, et al. Hampton G, et al. Among authors: senger g. Genomics. 1991 Oct;11(2):247-51. doi: 10.1016/0888-7543(91)90130-7. Genomics. 1991. PMID: 1663069

4

New markers for the neurofibromatosis-2 region generated by microdissection of chromosome 22.

Fiedler W, Claussen U, Lüdecke HJ, Senger G, Horsthemke B, Geurts Van Kessel A, Goertzen W, Fahsold R. Fiedler W, et al. Among authors: senger g. Genomics. 1991 Jul;10(3):786-91. doi: 10.1016/0888-7543(91)90464-p. Genomics. 1991. PMID: 1909684

5

Construction and characterization of band-specific DNA libraries.

Lüdecke HJ, Senger G, Claussen U, Horsthemke B. Lüdecke HJ, et al. Among authors: senger g. Hum Genet. 1990 May;84(6):512-6. doi: 10.1007/BF00210800. Hum Genet. 1990. PMID: 2159949

6

Microdissection of banded human chromosomes.

Senger G, Lüdecke HJ, Horsthemke B, Claussen U. Senger G, et al. Hum Genet. 1990 May;84(6):507-11. doi: 10.1007/BF00210799. Hum Genet. 1990. PMID: 2186996

7

Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences.

Buiting K, Neumann M, Lüdecke HJ, Senger G, Claussen U, Antich J, Passarge E, Horsthemke B. Buiting K, et al. Among authors: senger g. Genomics. 1990 Mar;6(3):521-7. doi: 10.1016/0888-7543(90)90481-9. Genomics. 1990. PMID: 2328991

8

Microdissection of the fragile X region.

MacKinnon RN, Hirst MC, Bell MV, Watson JE, Claussen U, Ludecke HJ, Senger G, Horsthemke B, Davies KE. MacKinnon RN, et al. Among authors: senger g. Am J Hum Genet. 1990 Aug;47(2):181-6. Am J Hum Genet. 1990. PMID: 2378345 Free PMC article.

9

Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndrome.

Lüdecke HJ, Burdiek R, Senger G, Claussen U, Passarge E, Horsthemke B. Lüdecke HJ, et al. Among authors: senger g. Hum Genet. 1989 Jul;82(4):327-9. doi: 10.1007/BF00273991. Hum Genet. 1989. PMID: 2567694

10

11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.

Puech A, Ahnine L, Lüdecke HJ, Senger G, Ivens A, Jeanpierre C, Little P, Horsthemke B, Claussen U, Jones C, et al. Puech A, et al. Among authors: senger g. Genomics. 1992 Aug;13(4):1274-80. doi: 10.1016/0888-7543(92)90046-u. Genomics. 1992. PMID: 1380484

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