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Human Mutation|June 30, 2000
Identification of PATCHED mutations in medulloblastomas by direct sequencingJ Dong, M R Gailani, S L Pomeroy, et al.The Laryngoscope|April 14, 1999
Mutational analyses of candidate genes in human squamous cell carcinomasA Petroianu, W L Boson, A E Bale, et al.The Journal of Pediatrics|September 15, 1999
Familial medullary thyroid carcinoma: presymptomatic diagnosis and management in childrenR A Heptulla, R P Schwartz, A E Bale, et al.American Journal of Human Genetics|May 1, 1994
Localization of the gene for the nevoid basal cell carcinoma syndromeA M Goldstein, C Stewart, A E Bale, et al.Genetics Research|March 8, 2016
Defining the polyposis/colorectal cancer phenotype associated with the Ashkenazi GREM1 duplication: counselling and management recommendationsJames Ziai, Ellen Matloff, Jaehyuk Choi, et al.Pediatric Neurology|September 28, 2016
Mitochondrial Membrane Protein-Associated Neurodegeneration Mimicking Juvenile Amyotrophic Lateral SclerosisJiyeon Kim, Yu-Hsien Liao, Cristian Ionita, et al.Physical Chemistry Chemical Physics : PCCP|October 2, 2009
A discharge-flow study of the kinetics of the reactions of IO with CH3O2 and CF3O2Catherine S E Bale, Carlos E Canosa-Mas, Dudley E Shallcross, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 1, 2004
Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patientsDoo Ho Choi, Min Hyuk Lee, Allen E Bale, et al.Cancer Research|September 5, 2006
Multiple endocrine neoplasia type 1 interacts with forkhead transcription factor CHES1 in DNA damage responseValeria Busygina, Molly C Kottemann, Kenneth L Scott, et al.Nature Clinical Practice. Oncology|October 5, 2006
Rhabdomyosarcoma, Wilms tumor, and deletion of the patched gene in Gorlin syndromeMariana M Cajaiba, Allen E Bale, Mayra Alvarez-Franco, et al.Pageof 13