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Clinical Endocrinology|December 14, 1999
In vitro and in vivo responses to short-term recombinant human insulin-like growth factor-1 (IGF-I) in a severely growth-retarded girl with ring chromosome 15 and deletion of a single allele for the type 1 IGF receptor geneL de Lacerda, J A Carvalho, B Stannard, et al.American Journal of Clinical Pathology|May 1, 1994
Correlation of pathologic features with clinical outcome in pediatric adrenocortical neoplasia. A study of a Brazilian population. Brazilian Group for Treatment of Childhood Adrenocortical TumorsM F Bugg, R C Ribeiro, P K Roberson, et al.The Journal of Clinical Investigation|March 1, 1996
A circulating, biologically inactive thyrotropin caused by a mutation in the beta subunit geneG Medeiros-Neto, D T Herodotou, S Rajan, et al.Human Mutation|September 8, 1999
Molecular analyses of the vasopressin type 2 receptor and aquaporin-2 genes in Brazilian kindreds with nephrogenic diabetes insipidusJ L Rocha, E Friedman, W Boson, et al.Proceedings of the National Academy of Sciences of the United States of America|August 2, 2001
An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinomaR C Ribeiro, F Sandrini, B Figueiredo, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 3, 2004
Clinical and outcome characteristics of children with adrenocortical tumors: a report from the International Pediatric Adrenocortical Tumor RegistryE Michalkiewicz, R Sandrini, B Figueiredo, et al.Journal of Medical Genetics|July 22, 2005
Penetrance of adrenocortical tumours associated with the germline TP53 R337H mutationB C Figueiredo, R Sandrini, G P Zambetti, et al.Pageof 2