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Nature Genetics|May 1, 1994
Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbours p53 gene mutationsN Bardeesy, D Falkoff, M J Petruzzi, et al.Genes, Chromosomes & Cancer|March 1, 1991
Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rareB Royer-Pokora, S Ragg, B Heckl-Ostreicher, et al.American Journal of Human Genetics|April 28, 2001
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tardaG E Tiller, V L Hannig, D Dozier, et al.Journal of Biomechanics|May 19, 2009
Biaxial cell stimulation: A mechanical validationF H Bieler, C E Ott, M S Thompson, et al.American Journal of Human Genetics|June 12, 1999
Identification of novel pro-alpha2(IX) collagen gene mutations in two families with distinctive oligo-epiphyseal forms of multiple epiphyseal dysplasiaP Holden, E G Canty, G R Mortier, et al.Nature Genetics|October 1, 1996
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN geneB Dittrich, K Buiting, B Korn, et al.Journal of Medical Genetics|June 1, 1996
Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasiaG A Wallis, B Rash, B Sykes, et al.Genomics|July 1, 1991
A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locusL M Davis, B Zabel, G Senger, et al.Human Molecular Genetics|April 18, 2000
LMX1B transactivation and expression in nail-patella syndromeS D Dreyer, R Morello, M S German, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1990
Somatic cell hybrid and long-range physical mapping of 11p13 microdissected genomic clonesL M Davis, G Senger, H J Lüdecke, et al.Pageof 18