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Human Mutation|June 16, 2005
Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidneyR Wieser, B Fritz, R Ullmann, et al.
American Journal of Medical Genetics|April 6, 2000
Molecular cytogenetic studies in three patients with partial trisomy 2p, including CGH from paraffin-embedded tissueA Aviram-Goldring, B Fritz, C Bartsch, et al.
Human Genetics|April 1, 1997
Microdeletion 22q11 in complex cardiovascular malformationsY Mehraein, C F Wippermann, I Michel-Behnke, et al.
Der Pathologe|March 1, 1996
[Consensus report: tissue handling in suspected Creutzfeldt-Jakob disease and other spongiform encephalopathies (prion diseases) in the human. European Union Biomed-1 Concerted Action]H Budka, A Aguzzi, P Brown, et al.
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