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Results: 1-9 |
Results: 9
FISH monitoring of 100 courses of human leukemias: The cytogenetic viewpoint
Authors: Gebhart, E Rosler, W Gramatzki, M Trautmann, U
Citation: E. Gebhart et al., FISH monitoring of 100 courses of human leukemias: The cytogenetic viewpoint, INT J ONCOL, 19(3), 2001, pp. 617-623
The cytogenetic view of standard comparative genomic hybridization (CGH): Deletions of 20q in human leukemia as a measure of the sensitivity of the technique
Authors: Brecevic, L Verdorfer, I Saul, W Trautmann, U Gebhart, E
Citation: L. Brecevic et al., The cytogenetic view of standard comparative genomic hybridization (CGH): Deletions of 20q in human leukemia as a measure of the sensitivity of the technique, ANTICANC R, 21(1A), 2001, pp. 89-92
Deletion 15q24-26 in prenatally detected diaphragmatic hernia: increasing evidence of a candidate region for diaphragmatic development
Authors: Schlembach, D Zenker, M Trautmann, U Ulmer, R Beinder, E
Citation: D. Schlembach et al., Deletion 15q24-26 in prenatally detected diaphragmatic hernia: increasing evidence of a candidate region for diaphragmatic development, PRENAT DIAG, 21(4), 2001, pp. 289-292
Comparative genomic hybridization-aided unraveling of complex karyotypes in human hematopoietic neoplasias
Authors: Verdorfer, I Brecevic, L Saul, W Schenker, B Kirsch, M Trautmann, U Helm, G Gramatzki, M Gebhart, E
Citation: I. Verdorfer et al., Comparative genomic hybridization-aided unraveling of complex karyotypes in human hematopoietic neoplasias, CANC GENET, 124(1), 2001, pp. 1-6
First known microdeletion within the Wolf-Hirschhorn-syndrome critical region refines genotype-phenotype correlation
Authors: Rauch, A Schellmoser, S Kraus, C Dorr, HG Trautmann, U Altherr, MR Pfeiffer, RA Reis, A
Citation: A. Rauch et al., First known microdeletion within the Wolf-Hirschhorn-syndrome critical region refines genotype-phenotype correlation, AM J MED G, 99(4), 2001, pp. 338-342
Delimiting the use of comparative genomic hybridization in human myeloid neoplastic disorders
Authors: Gebhart, E Verdorfer, I Saul, W Trautmann, U Brecevic, L
Citation: E. Gebhart et al., Delimiting the use of comparative genomic hybridization in human myeloid neoplastic disorders, INT J ONCOL, 16(6), 2000, pp. 1099-1105
FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primates
Authors: Shan, ZH Zabel, B Trautmann, U Hillig, U Ottolenghi, C Wang, YY Haaf, T
Citation: Zh. Shan et al., FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primates, EUR J HUM G, 8(3), 2000, pp. 167-173
Prenatal diagnosis of heterokaryotypic mosaic twins discordant for fetal sex
Authors: Schmid, O Trautmann, U Ashour, H Ulmer, R Pfeiffer, RA Beinder, E
Citation: O. Schmid et al., Prenatal diagnosis of heterokaryotypic mosaic twins discordant for fetal sex, PRENAT DIAG, 20(12), 2000, pp. 999-1003
Defective sexual development in an infant with 46, XY, der(9)t(8;9)(q23.1;p23)mat
Authors: Pfeiffer, RA Rauch, A Trautmann, U Dorr, HG Hiort, O Scherer, G Rosch, G Papadopoulos, T Van der Hardt, K Lachmann, E
Citation: Ra. Pfeiffer et al., Defective sexual development in an infant with 46, XY, der(9)t(8;9)(q23.1;p23)mat, EUR J PED, 158(3), 1999, pp. 213-216
Risultati: 1-9 |