Analysis of the Prader-Willi Syndrome Chromosome Region Using Quantitative Microsphere Hybridization (QMH) Array

Por Newkirk, H.L., Bittel, D.C., Butler, M.G.
Publicado no Am J Med Genet A (2008)

Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH

Por Bittel, D.C., Yu, S., Newkirk, H., Kibiryeva, N., Holt, S., Butler, M.G., Cooley, L.D.
Publicado em 2009

Comparison of X-chromosome inactivation patterns in multiple tissues from human females

Por Bittel, D C, Theodoro, M F, Kibiryeva, N, Fischer, W, Talebizadeh, Z, Butler, M G
Publicado no J Med Genet (2007)

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism

Por Talebizadeh, Z, Lam, D Y, Theodoro, M F, Bittel, D C, Lushington, G H, Butler, M G
Publicado em 2006

Single-amino acid substitutions eliminate lysine inhibition of maize dihydrodipicolinate synthase.

Por Shaver, J M, Bittel, D C, Sellner, J M, Frisch, D A, Somers, D A, Gengenbach, B G
Publicado em 1996