Douglas C. Bittel
Children's Mercy Hospitals and Clinics
University of Missouri-Kansas City School of Medicine
Kansas City
MO 64108
USA
Name/email consistency: high
- Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH. Bittel, D.C., Yu, S., Newkirk, H., Kibiryeva, N., Holt, A., Butler, M.G., Cooley, L.D. Cytogenet. Genome Res. (2009)
- Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD. Bittel, D.C., Kibiryeva, N., Talebizadeh, Z., Driscoll, D.J., Butler, M.G. Genomics (2005)
- Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology. Bittel, D.C., Butler, M.G. Expert. Rev. Mol. Med (2005)