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Ugeskrift for Laeger|November 16, 1992
[Identification of Y chromosome material in an XX male by means of fluorescent in situ hybridization]C A Brandt, J Hindkjaer, H Strømkjaer, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|August 1, 1993
Molecular cytogenetics: applications in clinical geneticsC A Brandt, J Hindkjaer, H Strømkjaer, et al.Clinical Genetics|December 1, 1996
Primed IN situ labelling (PRINS) as a rational procedure for identification of marker chromosomes using a panel of primers differentially tagging the human chromosomesJ Hindkjaer, C A Brandt, H Strømkjaer, et al.Clinical Genetics|August 1, 1993
Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21B Hertz, C A Brandt, M B Petersen, et al.Clinical Genetics|July 1, 1997
A patient with Edwards syndrome caused by a rare pseudodicentric chromosome 18 of paternal originC H Gravholt, M Bugge, H Strømkjaer, et al.Journal of Medical Genetics|February 1, 1994
Pseudodicentric chromosome 18 diagnosed by chromosome painting and primed in situ labelling (PRINS)C A Brandt, B Djernes, H Strømkjaer, et al.Human Genetics|September 1, 1997
A de nevo complex t(7;13;8) translocation with a deletion in the TRPS gene regionC A Brandt, H J Lüdecke, J Hindkjaer, et al.Pageof 1