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A Jauch

Showing results (61-70 of 109) with videos related to

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American Journal of Medical Genetics|May 8, 2000
Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal originG Oner, A Jauch, T Eggermann, et al.
Cancer Research|July 15, 1994
Chromosomal gains and losses in uveal melanomas detected by comparative genomic hybridizationM R Speicher, G Prescher, S du Manoir, et al.
The American Journal of Pathology|June 1, 1995
Correlation of microscopic phenotype with genotype in a formalin-fixed, paraffin-embedded testicular germ cell tumor with universal DNA amplification, comparative genomic hybridization, and interphase cytogeneticsM R Speicher, A Jauch, H Walt, et al.
Human Genetics|December 1, 1993
A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clonesS Popp, A Jauch, D Schindler, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|September 1, 1994
The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibraryJ Wienberg, A Jauch, H J Lüdecke, et al.
American Journal of Medical Genetics|May 8, 1999
Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3S Spranger, S Schiller, A Jauch, et al.
Cancer Genetics and Cytogenetics|September 1, 1997
Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell linesN Van Roy, A Jauch, M Van Gele, et al.
Blood|May 15, 1994
Detection of 14q32 translocations in B-cell malignancies by in situ hybridization with yeast artificial chromosome clones containing the human IgH gene locusM Taniwaki, F Matsuda, A Jauch, et al.
Cancer Genetics and Cytogenetics|October 24, 2001
Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogeneticsM Granzow, S Popp, S Weber, et al.
The Journal of Pathology|July 9, 1999
Chromosomal abnormalities in renal cell neoplasms associated with acquired renal cystic disease. A series studied by comparative genomic hybridization and fluorescence in situ hybridizationJ Gronwald, A S Baur, H Holtgreve-Grez, et al.
Pageof 11

Showing results (61-70 of 109) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|May 8, 2000
Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal originG Oner, A Jauch, T Eggermann, et al.
Cancer Research|July 15, 1994
Chromosomal gains and losses in uveal melanomas detected by comparative genomic hybridizationM R Speicher, G Prescher, S du Manoir, et al.
The American Journal of Pathology|June 1, 1995
Correlation of microscopic phenotype with genotype in a formalin-fixed, paraffin-embedded testicular germ cell tumor with universal DNA amplification, comparative genomic hybridization, and interphase cytogeneticsM R Speicher, A Jauch, H Walt, et al.
Human Genetics|December 1, 1993
A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clonesS Popp, A Jauch, D Schindler, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|September 1, 1994
The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibraryJ Wienberg, A Jauch, H J Lüdecke, et al.
American Journal of Medical Genetics|May 8, 1999
Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3S Spranger, S Schiller, A Jauch, et al.
Cancer Genetics and Cytogenetics|September 1, 1997
Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell linesN Van Roy, A Jauch, M Van Gele, et al.
Blood|May 15, 1994
Detection of 14q32 translocations in B-cell malignancies by in situ hybridization with yeast artificial chromosome clones containing the human IgH gene locusM Taniwaki, F Matsuda, A Jauch, et al.
Cancer Genetics and Cytogenetics|October 24, 2001
Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogeneticsM Granzow, S Popp, S Weber, et al.
The Journal of Pathology|July 9, 1999
Chromosomal abnormalities in renal cell neoplasms associated with acquired renal cystic disease. A series studied by comparative genomic hybridization and fluorescence in situ hybridizationJ Gronwald, A S Baur, H Holtgreve-Grez, et al.
Pageof 11