Christopher M. Stanczak

Deletion mapping in Xp21 for patients with complex glycerol kinase deficiency using SNP mapping arrays

S. Nelson, Zugen Chen, E. McCabe, 2007, Human mutation.

Representational oligonucleotide microarray analysis (ROMA) and comparison of binning and change‐point methods of analysis: application to detection of del22q11.2 (DiGeorge) Syndrome

M. Suchard, Zugen Chen, S. Mcghee, 2008, Human mutation.