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Clinical Genetics|August 17, 2000
Cortical dysgenesis in 2 patients with chromosome 22q11 deletionL M Bird, P ScamblerAmerican Journal of Human Genetics|January 1, 1986
The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4M Farrall, P Scambler, P North, et al.Journal of Medical Genetics|September 1, 1995
Monozygotic twins with chromosome 22q11 deletion and discordant phenotypeJ Goodship, I Cross, P Scambler, et al.Gene|April 3, 1998
Isolation and genomic characterization of the TUPLE1/HIRA gene of the pufferfish Fugu rubripesR Llevadot, X Estivill, P Scambler, et al.Medical Engineering & Physics|August 13, 2010
Mitral valve dynamics in structural and fluid-structure interaction modelsK D Lau, V Diaz, P Scambler, et al.Genomics|February 10, 1995
Cloning and mapping of murine Nfe2l1J McKie, K Johnstone, M G Mattei, et al.Journal of Medical Genetics|October 1, 1993
DiGeorge syndrome: part of CATCH 22D I Wilson, J Burn, P Scambler, et al.Oncogene|August 5, 1998
Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumourR G Grundy, J Pritchard, P Scambler, et al.Journal of Biomechanics|July 20, 2011
Fluid-structure interaction study of the edge-to-edge repair technique on the mitral valveK D Lau, V Díaz-Zuccarini, P Scambler, et al.British Journal of Cancer|November 20, 1998
Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumourR G Grundy, J Pritchard, P Scambler, et al.Pageof 197