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Human Heredity|April 3, 2008
A family-based likelihood ratio test for general pedigree structures that allows for genotyping error and missing dataYang Yang, Carol A Wise, Derek Gordon, et al.Studies in Health Technology and Informatics|October 2, 2004
Positional cloning strategies for idiopathic scoliosisStavros Bashiardes, Rose Veile, Carol A Wise, et al.Current Genomics|May 9, 2009
Understanding genetic factors in idiopathic scoliosis, a complex disease of childhoodCarol A Wise, Xiaochong Gao, Scott Shoemaker, et al.Spine Deformity|December 9, 2016
Genomic Analyses of Patients With Unexplained Early-Onset ScoliosisXiaochong Gao, Garrett Gotway, Karl Rathjen, et al.Clinical Orthopaedics and Related Research|May 31, 2007
Apoptotic gene analysis in idiopathic talipes equinovarus (clubfoot)Audrey R Ester, Gayle Tyerman, Carol A Wise, et al.BMC Bioinformatics|January 24, 2012
TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association dataDouglas Londono, Steven Buyske, Stephen J Finch, et al.The Journal of Bone and Joint Surgery. American Volume|April 1, 2025
Molecular Evidence Supporting MEK Inhibitor Therapy in NF1 PseudarthrosisNandina Paria, Ila Oxendine, David Podeszwa, et al.Nature Communications|September 4, 2014
ptk7 mutant zebrafish models of congenital and idiopathic scoliosis implicate dysregulated Wnt signalling in diseaseMadeline Hayes, Xiaochong Gao, Lisa X Yu, et al.Human Molecular Genetics|October 27, 2012
Somatic gain-of-function mutations in PIK3CA in patients with macrodactylyJonathan J Rios, Nandina Paria, Dennis K Burns, et al.Clinical Case Reports|September 5, 2020
Novel homozygous variant in WISP3 in a family with unrecognized progressive pseudorheumatoid dysplasiaChandreshkumar Patel, Anas M Khanshour, David Wilkes, et al.Pageof 8