Senger G - Search Results

1

Characterization of Small Marker Chromosomes (SMC) by Recently Developed Molecular Cytogenetic Approaches.

Liehr T, Nietzel A, Starke H, Heller A, Weise A, Kuechler A, Senger G, Ebner S, Martin T, Stumm M, Wegner R, Tönnies H, Hoppe C, Claussen U, Von Eggeling F. Liehr T, et al. Among authors: senger g. J Assoc Genet Technol. 2003;29(1):5-10. J Assoc Genet Technol. 2003. PMID: 15213421 No abstract available.

2

Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.

Liehr T, Starke H, Senger G, Melotte C, Weise A, Vermeesch JR. Liehr T, et al. Among authors: senger g. Am J Med Genet A. 2006 Jan 1;140(1):46-51. doi: 10.1002/ajmg.a.31048. Am J Med Genet A. 2006. PMID: 16333826 Review.

3

Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review.

Heller A, Seidel J, Hübler A, Starke H, Beensen V, Senger G, Rocchi M, Wirth J, Chudoba I, Claussen U, Liehr T. Heller A, et al. Among authors: senger g. J Med Genet. 2000 Jul;37(7):529-32. doi: 10.1136/jmg.37.7.529. J Med Genet. 2000. PMID: 10882757 Free PMC article.

4

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements.

Starke H, Seidel J, Henn W, Reichardt S, Volleth M, Stumm M, Behrend C, Sandig KR, Kelbova C, Senger G, Albrecht B, Hansmann I, Heller A, Claussen U, Liehr T. Starke H, et al. Among authors: senger g. Eur J Hum Genet. 2002 Dec;10(12):790-800. doi: 10.1038/sj.ejhg.5200889. Eur J Hum Genet. 2002. PMID: 12461685

5

Evidence for a new microdeletion syndrome in 15q21.

Liehr T, Starke H, Heller A, Weise A, Beensen V, Senger G, Kittner G, Prechtel M, Claussen U, Seidel J. Liehr T, et al. Among authors: senger g. Int J Mol Med. 2003 May;11(5):575-7. doi: 10.3892/ijmm.11.5.575. Int J Mol Med. 2003. PMID: 12684692

6

A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.

Seidel J, Heller A, Senger G, Starke H, Chudoba I, Kelbova C, Tönnies H, Neitzel H, Haase C, Beensen V, Zintl F, Claussen U, Liehr T. Seidel J, et al. Among authors: senger g. Eur J Pediatr. 2003 Sep;162(9):582-8. doi: 10.1007/s00431-003-1254-3. Epub 2003 Jun 19. Eur J Pediatr. 2003. PMID: 12819962 Review.

7

Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias.

Heller A, Chudoba I, Bleck C, Senger G, Claussen U, Liehr T. Heller A, et al. Among authors: senger g. Int J Oncol. 2000 Mar;16(3):461-8. Int J Oncol. 2000. PMID: 10675476

8

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

9

Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB).

Starke H, Senger G, Kossakiewicz M, Tittelbach H, Rau D, Rubtsov N, Trifonov V, Heller A, Hartmann I, Claussen U, Liehr T. Starke H, et al. Among authors: senger g. Prenat Diagn. 2001 Dec;21(12):1049-52. doi: 10.1002/pd.192. Prenat Diagn. 2001. PMID: 11746162

10

Construction of band-specific DNA-libraries by microdissection of GTG-banded human chromosomes and universal enzymatic DNA amplification.

Claussen U, Ludecke HJ, Senger G, Horsthemke B. Claussen U, et al. Among authors: senger g. Bull Assoc Anat (Nancy). 1991 Jun;75(229):133-6. Bull Assoc Anat (Nancy). 1991. PMID: 1777702 No abstract available.

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