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Human Molecular Genetics|March 1, 1995
DNA binding capacity of the WT1 protein is abolished by Denys-Drash syndrome WT1 point mutationsM Little, G Holmes, W Bickmore, et al.Human Genetics|June 1, 1986
Use of catalase polymorphisms in the study of sporadic aniridiaP Boyd, V van Heyningen, A Seawright, et al.Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Complete sequencing of the Fugu WAGR region from WT1 to PAX6: dramatic compaction and conservation of synteny with human chromosome 11p13C Miles, G Elgar, E Coles, et al.Nature Genetics|August 1, 1992
The human PAX6 gene is mutated in two patients with aniridiaT Jordan, I Hanson, D Zaletayev, et al.Current Opinion in Genetics & Development|June 1, 1996
Transcription factors in diseaseD Engelkamp, V van HeyningenImmunology Today|October 8, 2014
An ordered sequence of expression of human MHC class-II antigens during B-cell maturation?K Guy, V van HeyningenCancer Research|April 10, 1999
Multiple roles for the Wilms' tumor suppressor, WT1R Davies, A Moore, A Schedl, et al.Trends in Genetics : TIG|January 1, 1992
Wilms' tumour: reconciling genetics and biologyV Van Heyningen, N D HastiePageof 97