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Results: 1-8 |
Results: 8
Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL)
Authors: Brown, J Saracoglu, K Uhrig, S Speicher, MR Eils, R Kearney, L
Citation: J. Brown et al., Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL), NAT MED, 7(4), 2001, pp. 497-501
New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization
Authors: Saracoglu, K Brown, J Kearney, L Uhrig, S Azofeifa, J Fauth, C Speicher, MR Eils, R
Citation: K. Saracoglu et al., New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization, CYTOMETRY, 44(1), 2001, pp. 7-15
Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative hybridization and multicolor bar coding (vol 80, pg 1031, 2000)
Authors: Speicher, MR Petersen, S Uhrig, S Jentsch, I Fauth, C Eils, R Petersen, I
Citation: Mr. Speicher et al., Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative hybridization and multicolor bar coding (vol 80, pg 1031, 2000), LAB INV, 80(8), 2000, pp. 1145-1145
Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative genomic hybridization, and multicolor bar coding
Authors: Speicher, MR Petersen, S Uhrig, S Jentsch, I Fauth, C Eils, R Petersen, I
Citation: Mr. Speicher et al., Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative genomic hybridization, and multicolor bar coding, LAB INV, 80(7), 2000, pp. 1031-1041
Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito andasymmetry
Authors: Schmidt, H Uhrig, S Lederer, G Murken, J Speicher, MR Schuffenhauer, S
Citation: H. Schmidt et al., Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito andasymmetry, J MED GENET, 37(10), 2000, pp. 804-806
Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3)
Authors: Holinski-Feder, E Reyniers, E Uhrig, S Golla, A Wauters, J Kroisel, P Bossuyt, P Rost, I Jedele, K Zierler, H Schwab, S Wildenauer, D Speicher, MR Willems, PJ Meitinger, T Kooy, RF
Citation: E. Holinski-feder et al., Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3), AM J HU GEN, 66(1), 2000, pp. 16-25
Multiplex-FISH for pre- and postnatal diagnostic applications
Authors: Uhrig, S Schuffenhauer, S Fauth, C Wirtz, A Daumer-Haas, C Apacik, C Cohen, M Muller-Navia, J Cremer, T Murken, J Speicher, MR
Citation: S. Uhrig et al., Multiplex-FISH for pre- and postnatal diagnostic applications, AM J HU GEN, 65(2), 1999, pp. 448-462
An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH)
Authors: Eils, R Uhrig, S Saracoglu, K Satzler, K Bolzer, A Petersen, I Chassery, JM Ganser, M Speicher, MR
Citation: R. Eils et al., An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH), CYTOG C GEN, 82(3-4), 1998, pp. 160-171
Risultati: 1-8 |