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Human Genetics|February 1, 1991
A molecular genetic approach to the identification of isochromosomes of chromosome 21L G Shaffer, C K Jackson-Cook, J M Meyer, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Array comparative genomic hybridization in global developmental delayM I Shevell, B A Bejjani, M Srour, et al.
American Journal of Medical Genetics|March 27, 1995
Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted regionE A Lindsay, F Greenberg, L G Shaffer, et al.
American Journal of Medical Genetics|August 1, 1992
Parental origin determination in thirty de novo Robertsonian translocationsL G Shaffer, C K Jackson-Cook, B A Stasiowski, et al.
American Journal of Medical Genetics|April 24, 1999
Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomyS A Berend, G L Feldman, C McCaskill, et al.
Cytogenetic and Genome Research|March 17, 2009
Benign copy number changes in clinical cytogenetic diagnostics by array CGHH Whitby, A Tsalenko, E Aston, et al.
The Journal of Molecular Diagnostics : JMD|March 29, 2001
Evidence by spectral karyotyping that 8q11.2 is nonrandomly involved in lipoblastomaZ Chen, C M Coffin, S Scott, et al.
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