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I McIntosh

Showing results (71-80 of 97) with videos related to

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Journal of Heterocyclic Chemistry|August 19, 2017
Synthesis and Investigation of Mixed μ-Opioid and δ-Opioid Agonists as Possible Bivalent Ligands for Treatment of PainRuben S Vardanyan, James P Cain, Saghar Mowlazadeh Haghighi, et al.
Human Heredity|March 1, 1997
No evidence of linkage for cleft lip with or without cleft palate to a marker near the transforming growth factor alpha locus in two populationsD F Wyszynski, N Maestri, A F Lewanda, et al.
American Journal of Human Genetics|August 1, 1992
Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileusA Hamosh, T M King, B J Rosenstein, et al.
Human Genetics|January 1, 1997
Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex familiesD F Wyszynski, N Maestri, I McIntosh, et al.
Nature Genetics|September 1, 1993
A type X collagen mutation causes Schmid metaphyseal chondrodysplasiaM L Warman, M Abbott, S S Apte, et al.
American Journal of Medical Genetics|January 24, 1998
Application of transmission disequilibrium tests to nonsyndromic oral clefts: including candidate genes and environmental exposures in the modelsN E Maestri, T H Beaty, J Hetmanski, et al.
Therapeutic Innovation & Regulatory Science|June 21, 2024
Patient and Public Perceptions in Canada About Decentralized and Hybrid Clinical Trials: "It's About Time we Bring Trials to People"Dawn P Richards, John Queenan, Linnea Aasen-Johnston, et al.
Nature Genetics|July 1, 1995
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasiaG A Bellus, I McIntosh, E A Smith, et al.
Statistics in Medicine|April 4, 2017
Extensions to Bayesian generalized linear mixed effects models for household tuberculosis transmissionAvery I McIntosh, Gheorghe Doros, Edward C Jones-López, et al.
American Journal of Human Genetics|February 1, 1995
Achondroplasia is defined by recurrent G380R mutations of FGFR3G A Bellus, T W Hefferon, R I Ortiz de Luna, et al.
Pageof 10

Showing results (71-80 of 97) with videos related to

Sort By:
Pageof 10
Journal of Heterocyclic Chemistry|August 19, 2017
Synthesis and Investigation of Mixed μ-Opioid and δ-Opioid Agonists as Possible Bivalent Ligands for Treatment of PainRuben S Vardanyan, James P Cain, Saghar Mowlazadeh Haghighi, et al.
Human Heredity|March 1, 1997
No evidence of linkage for cleft lip with or without cleft palate to a marker near the transforming growth factor alpha locus in two populationsD F Wyszynski, N Maestri, A F Lewanda, et al.
American Journal of Human Genetics|August 1, 1992
Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileusA Hamosh, T M King, B J Rosenstein, et al.
Human Genetics|January 1, 1997
Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex familiesD F Wyszynski, N Maestri, I McIntosh, et al.
Nature Genetics|September 1, 1993
A type X collagen mutation causes Schmid metaphyseal chondrodysplasiaM L Warman, M Abbott, S S Apte, et al.
American Journal of Medical Genetics|January 24, 1998
Application of transmission disequilibrium tests to nonsyndromic oral clefts: including candidate genes and environmental exposures in the modelsN E Maestri, T H Beaty, J Hetmanski, et al.
Therapeutic Innovation & Regulatory Science|June 21, 2024
Patient and Public Perceptions in Canada About Decentralized and Hybrid Clinical Trials: "It's About Time we Bring Trials to People"Dawn P Richards, John Queenan, Linnea Aasen-Johnston, et al.
Nature Genetics|July 1, 1995
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasiaG A Bellus, I McIntosh, E A Smith, et al.
Statistics in Medicine|April 4, 2017
Extensions to Bayesian generalized linear mixed effects models for household tuberculosis transmissionAvery I McIntosh, Gheorghe Doros, Edward C Jones-López, et al.
American Journal of Human Genetics|February 1, 1995
Achondroplasia is defined by recurrent G380R mutations of FGFR3G A Bellus, T W Hefferon, R I Ortiz de Luna, et al.
Pageof 10