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Genetic Epidemiology|January 30, 2004
What SNP genotyping errors are most costly for genetic association studies?Sun Jung Kang, Derek Gordon, Stephen J Finch
American Journal of Medical Genetics. Part A|December 12, 2002
Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasiaJudith L Ross, Gary Bellus, Charles I Scott, et al.
American Journal of Medical Genetics. Part A|March 31, 2007
Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD)Angel Campos-Barros, Sara Benito-Sanz, Judith L Ross, et al.
Journal of Pediatric Surgery|November 21, 2007
Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's diseaseJuan C Prieto, Nilda M Garcia, Frederick F Elder, et al.
Developmental Disabilities Research Reviews|December 17, 2009
An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndromeJudith L Ross, Martha P D Zeger, Harvey Kushner, et al.
Bioinformatics (Oxford, England)|August 27, 2005
PAWE-3D: visualizing power for association with error in case-control genetic studies of complex traitsDerek Gordon, Chad Haynes, Jon Blumenfeld, et al.
Annals of Human Genetics|April 7, 2009
The cost effectiveness of duplicate genotyping for testing genetic associationNathan Tintle, Derek Gordon, Dirk Van Bruggen, et al.
BMJ Case Reports|June 15, 2012
Use of cetrorelix in the investigation of testosterone excess in a postmenopausal womanDonna J Chantler, Derek Gordon, David Millan, et al.
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