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BMC Bioinformatics|January 20, 2006
Analysis and visualization of chromosomal abnormalities in SNP data with SNPscanJason C Ting, Ying Ye, George H Thomas, et al.BMC Medical Genetics|September 19, 2009
Locations and patterns of meiotic recombination in two-generation pedigreesJason C Ting, Elisha D O Roberson, Duane G Currier, et al.Human Molecular Genetics|February 21, 2002
KRIT1 association with the integrin-binding protein ICAP-1: a new direction in the elucidation of cerebral cavernous malformations (CCM1) pathogenesisJon S Zawistowski, Ilya G Serebriiskii, Maximilian F Lee, et al.Human Molecular Genetics|October 2, 2003
Multiple quantitative trait loci modify the heart failure phenotype in murine cardiomyopathyPhilippe Le Corvoisier, Hyun-Young Park, Kerri M Carlson, et al.Genetics|September 7, 2019
Novel Neuroprotective Loci Modulating Ischemic Stroke Volume in Wild-Derived Inbred Mouse StrainsHan Kyu Lee, Samuel J Widmayer, Min-Nung Huang, et al.Development (Cambridge, England)|March 3, 2004
Ccm1 is required for arterial morphogenesis: implications for the etiology of human cavernous malformationsKevin J Whitehead, Nicholas W Plummer, Jennifer A Adams, et al.Journal of Child Neurology|November 1, 2012
Importance of utilizing a sensitive free thyroxine assay in Sturge-Weber syndromeLaila Siddique, Aditya Sreenivasan, Anne M Comi, et al.Archives of Neurology|December 14, 2005
Sturge-Weber syndrome associated with other abnormalities: a medical record and literature reviewAnne M Comi, Paulomi Mehta, Laura A Hatfield, et al.Annual Review of Genetics|September 11, 2020
Mosaicism in Human Health and DiseaseJeremy Thorpe, Ikeoluwa A Osei-Owusu, Bracha Erlanger Avigdor, et al.Plos One|May 15, 2008
Efficient array-based identification of novel cardiac genes through differentiation of mouse ESCsRonald A Miller, Nicolas Christoforou, Jonathan Pevsner, et al.Pageof 27