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I McIntosh

Showing results (31-40 of 97) with videos related to

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Annals of Clinical Biochemistry|March 1, 1992
Variation of sweat sodium and chloride with age in cystic fibrosis and normal populations: further investigations in equivocal casesJ M Kirk, M Keston, I McIntosh, et al.
Journal of Medical Genetics|March 8, 2003
Nail patella syndrome: a review of the phenotype aided by developmental biologyE Sweeney, A Fryer, R Mountford, et al.
Journal of the Royal Society of Medicine|January 1, 1991
Cystic fibrosis: the new geneticsD J Brock, A E Shrimpton, C Jones, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Deletion of a branch-point consensus sequence in the LMX1B gene causes exon skipping in a family with nail patella syndromeJ D Hamlington, M V Clough, J A Dunston, et al.
American Journal of Human Genetics|September 14, 2001
Identification of TSIX, encoding an RNA antisense to human XIST, reveals differences from its murine counterpart: implications for X inactivationB R Migeon, A K Chowdhury, J A Dunston, 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.
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.
Pageof 10

Showing results (31-40 of 97) with videos related to

Sort By:
Pageof 10
Annals of Clinical Biochemistry|March 1, 1992
Variation of sweat sodium and chloride with age in cystic fibrosis and normal populations: further investigations in equivocal casesJ M Kirk, M Keston, I McIntosh, et al.
Journal of Medical Genetics|March 8, 2003
Nail patella syndrome: a review of the phenotype aided by developmental biologyE Sweeney, A Fryer, R Mountford, et al.
Journal of the Royal Society of Medicine|January 1, 1991
Cystic fibrosis: the new geneticsD J Brock, A E Shrimpton, C Jones, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Deletion of a branch-point consensus sequence in the LMX1B gene causes exon skipping in a family with nail patella syndromeJ D Hamlington, M V Clough, J A Dunston, et al.
American Journal of Human Genetics|September 14, 2001
Identification of TSIX, encoding an RNA antisense to human XIST, reveals differences from its murine counterpart: implications for X inactivationB R Migeon, A K Chowdhury, J A Dunston, 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.
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.
Pageof 10