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I McIntosh

Showing results (11-20 of 97) with videos related to

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Human Mutation|October 23, 2001
Twenty-two novel LMX1B mutations identified in nail patella syndrome (NPS) patientsJ D Hamlington, C Jones, I McIntosh
Human Mutation|January 1, 1995
Concentration of mutations causing Schmid metaphyseal chondrodysplasia in the C-terminal noncollagenous domain of type X collagenI McIntosh, M H Abbott, C A Francomano
American Journal of Mental Deficiency|July 1, 1973
Ethnic background, measured intelligence, and adaptive behavior scores in mentally retarded childrenJ Adams, E I McIntosh, B L Weade
Cell Structure and Function|July 8, 2000
The pleiotropic effects of fibroblast growth factor receptors in mammalian developmentI McIntosh, G A Bellus, E W Jab
Human Mutation|November 26, 1999
Restricted distribution of loss-of-function mutations within the LMX1B genes of nail-patella syndrome patientsM V Clough, J D Hamlington, I McIntosh
Journal of Medical Genetics|May 1, 1991
The incidence of different cystic fibrosis mutations in the Scottish population: effects on prenatal diagnosis and genetic counsellingA E Shrimpton, I McIntosh, D J Brock
Molecular and Cellular Probes|August 1, 1992
Detection of Pseudomonas aeruginosa in sputum from cystic fibrosis patients by the polymerase chain reactionI McIntosh, J R Govan, D J Brock
Current Opinion in Genetics & Development|June 1, 1996
Bone dysplasias in man: molecular insightsC A Francomano, I McIntosh, D J Wilkin
Vertex (Buenos Aires, Argentina)|October 31, 2002
[A pilot community study of subjective memory in over and under 65 years old]I McIntosh, J Grant, H Wilkinson, et al.
Lancet (London, England)|December 9, 1989
Frequency of delta F508 mutation on cystic fibrosis chromosomes in UKI McIntosh, M L Lorenzo, D J Brock
Pageof 10

Showing results (11-20 of 97) with videos related to

Sort By:
Pageof 10
Human Mutation|October 23, 2001
Twenty-two novel LMX1B mutations identified in nail patella syndrome (NPS) patientsJ D Hamlington, C Jones, I McIntosh
Human Mutation|January 1, 1995
Concentration of mutations causing Schmid metaphyseal chondrodysplasia in the C-terminal noncollagenous domain of type X collagenI McIntosh, M H Abbott, C A Francomano
American Journal of Mental Deficiency|July 1, 1973
Ethnic background, measured intelligence, and adaptive behavior scores in mentally retarded childrenJ Adams, E I McIntosh, B L Weade
Cell Structure and Function|July 8, 2000
The pleiotropic effects of fibroblast growth factor receptors in mammalian developmentI McIntosh, G A Bellus, E W Jab
Human Mutation|November 26, 1999
Restricted distribution of loss-of-function mutations within the LMX1B genes of nail-patella syndrome patientsM V Clough, J D Hamlington, I McIntosh
Journal of Medical Genetics|May 1, 1991
The incidence of different cystic fibrosis mutations in the Scottish population: effects on prenatal diagnosis and genetic counsellingA E Shrimpton, I McIntosh, D J Brock
Molecular and Cellular Probes|August 1, 1992
Detection of Pseudomonas aeruginosa in sputum from cystic fibrosis patients by the polymerase chain reactionI McIntosh, J R Govan, D J Brock
Current Opinion in Genetics & Development|June 1, 1996
Bone dysplasias in man: molecular insightsC A Francomano, I McIntosh, D J Wilkin
Vertex (Buenos Aires, Argentina)|October 31, 2002
[A pilot community study of subjective memory in over and under 65 years old]I McIntosh, J Grant, H Wilkinson, et al.
Lancet (London, England)|December 9, 1989
Frequency of delta F508 mutation on cystic fibrosis chromosomes in UKI McIntosh, M L Lorenzo, D J Brock
Pageof 10