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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.Human Genetics|October 30, 1999
Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor geneK R Bowles, J Gibson, J Wu, et al.Human Molecular Genetics|March 1, 1995
Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith-Wiedemann syndromeF Z Bischoff, G L Feldman, C McCaskill, 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.Prenatal Diagnosis|September 1, 1995
Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicismC Jones, C Booth, D Rita, 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.Pageof 22