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Genomics|February 1, 1991
The Marfan syndrome locus: confirmation of assignment to chromosome 15 and identification of tightly linked markers at 15q15-q21.3H C Dietz, R E Pyeritz, B D Hall, et al.Journal of Pediatric Orthopedics|August 25, 2001
The hip in Stickler syndromeP S Rose, N U Ahn, H P Levy, et al.Journal of the American Chemical Society|June 1, 2006
Heterogeneously catalyzed asymmetric C=C hydrogenation: origin of enantioselectivity in the proline-directed Pd/isophorone systemAlexander I McIntosh, David J Watson, Jonathan W Burton, et al.Human Molecular Genetics|April 1, 1992
Three novel mutations in the cystic fibrosis gene detected by chemical cleavage: analysis of variant splicing and a nonsense mutationC T Jones, I McIntosh, M Keston, et al.Annals of Human Genetics|January 11, 2005
Phenotype severity and genetic variation at the disease locus: an investigation of nail dysplasia in the nail patella syndromeJ A Dunston, S Lin, J W Park, et al.Genomics|February 10, 1995
COL5A1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers-Danlos Syndrome type IID S Greenspan, H Northrup, K S Au, et al.American Journal of Medical Genetics|March 3, 1998
Association between homeobox-containing gene MSX1 and the occurrence of limb deficiencyS J Hwang, T H Beaty, I McIntosh, et al.Nature Genetics|February 1, 1996
Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndromeS Sood, Z A Eldadah, W L Krause, et al.Annals of Human Genetics|July 6, 2005
Nail patella syndrome revisited: 50 years after linkageI McIntosh, J A Dunston, L Liu, et al.Chemical Society Reviews|December 7, 2011
Terahertz spectroscopy: a powerful new tool for the chemical sciences?Alexander I McIntosh, Bin Yang, Stephen M Goldup, et al.Pageof 17