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Annales De Genetique|January 1, 1994
Interstitial deletion 12p13.1-13.3 in a mildly retarded infant with unilateral ectrodactylyU Trautmann, R A PfeifferAnnales De Genetique|January 1, 1992
Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3R A Pfeiffer, G Legat, U TrautmannZeitschrift Fur Die Gesamte Innere Medizin Und Ihre Grenzgebiete|June 1, 1981
[The analysis of chromosomes today: aspects of the technic with indications and importance of the method]J Mücke, K R Sandig, U TrautmannAmerican Journal of Medical Genetics|May 3, 1996
Clinical and molecular cytogenetic observations in three cases of "trisomy 12p syndrome"A Rauch, U Trautmann, R A PfeifferClinical Genetics|June 1, 1996
Deletion or triplication of the alpha 3 (VI) collagen gene in three patients with 2q37 chromosome aberrations and symptoms of collagen-related disordersA Rauch, R A Pfeiffer, U TrautmannKlinische Padiatrie|September 1, 1983
[13q syndrome--partial monosomy of the long arm of chromosome 13]J Mücke, K R Sandig, U TrautmannClinical Genetics|August 1, 1992
Typical and partial cat eye syndrome: identification of the marker chromosome by FISHT Liehr, R A Pfeiffer, U TrautmannAnnales De Genetique|January 1, 1991
Interstitial deletion of chromosome 9q with coexistence of the deleted segment as a ring chromosome. A case reportR A Pfeiffer, U Trautmann, R Hirmer-StollAnticancer Research|September 1, 1993
Chromosomal heterogeneity of aneuploid leukemic cell populations detected by conventional karyotyping and by fluorescence in situ hybridization (FISH)E Gebhart, U Trautmann, S Reichardt, et al.International Journal of Oncology|August 9, 2001
FISH monitoring of 100 courses of human leukemias: the cytogenetic viewpointE Gebhart, W Rösler, M Gramatzki, et al.Pageof 5