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American Journal of Medical Genetics|April 10, 1995
De novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic, and molecular characterizationE A Lindsay, L G Shaffer, R Carrozzo, et al.
The Journal of Urology|July 1, 1993
Use of fluorescent in situ hybridization for deoxyribonucleic acid ploidy analysis of prostatic adenocarcinomaD L Persons, D J Gibney, J A Katzmann, et al.
American Journal of Medical Genetics|January 2, 1996
Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblingsK M Hegmann, A S Spikes, A Orr-Urtreger, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Estimates of aneuploidy using multicolor fluorescence in situ hybridization on human spermF Z Bischoff, D D Nguyen, K J Burt, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1AC D Kashork, K S Chen, J R Lupski, et al.
Cytogenetics and Cell Genetics|January 1, 1996
The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridizationK A Leppig, D Viskochil, S Neil, et al.
Molecular Genetics and Metabolism|April 5, 2001
Identification of a human brain-specific gene, calneuron 1, a new member of the calmodulin superfamilyY Q Wu, X Lin, C M Liu, et al.
Human Genetics|January 1, 1996
A clinical and molecular study of mosaicism for trisomy 17L G Shaffer, C McCaskill, J H Hersh, et al.
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