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Human Molecular Genetics|August 1, 1993
Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locusM Sanson, C Marineau, C Desmaze, et al.Nature|September 10, 1992
Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumoursO Delattre, J Zucman, B Plougastel, et al.American Journal of Human Genetics|December 1, 1993
Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial casesC Desmaze, M Prieur, F Amblard, et al.Genes, Chromosomes & Cancer|November 1, 1992
Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpointsJ Zucman, O Delattre, C Desmaze, et al.Human Molecular Genetics|April 1, 1995
Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinityS Demczuk, R Aledo, J Zucman, et al.Nature|June 10, 1993
Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2G A Rouleau, P Merel, M Lutchman, et al.The EMBO Journal|December 1, 1993
Combinatorial generation of variable fusion proteins in the Ewing family of tumoursJ Zucman, T Melot, C Desmaze, et al.Human Molecular Genetics|December 1, 1995
Oncogenic conversion of a novel orphan nuclear receptor by chromosome translocationY Labelle, J Zucman, G Stenman, et al.Pageof 3