1. Diagnostic testing for Prader-Willi and Angelman syndromes: Report of the ASHG/ACMG Test and Technology Transfer Committee;Am J Hum Genet,1996
2. Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3;Breuning;Am J Hum Genet,1993
3. The human homologue of the Drosophila melanogaster flightless-I gene (fliI) maps within the Smith-Magenis microdeletion critical region in 17p11.2;Chen;Am J Hum Genet,1995
4. Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome;Delach;Am J Med Genet,1994
5. Routine diagnosis of DiGeorge syndrome by fluorescence in situ hybridization;Desmaze;Hum Genet,1993