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Human Mutation
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October 23, 2001
Twenty-two novel LMX1B mutations identified in nail patella syndrome (NPS) patients
J 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 collagen
I 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 children
J Adams, E I McIntosh, B L Weade
Cell Structure and Function
|
July 8, 2000
The pleiotropic effects of fibroblast growth factor receptors in mammalian development
I 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 patients
M 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 counselling
A 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 reaction
I McIntosh, J R Govan, D J Brock
Current Opinion in Genetics & Development
|
June 1, 1996
Bone dysplasias in man: molecular insights
C 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 UK
I McIntosh, M L Lorenzo, D J Brock
Page
of 10
Search research articles
Search
Showing results (11-20 of 97) with videos related to
Sort By:
Page
of 10
Human Mutation
|
October 23, 2001
Twenty-two novel LMX1B mutations identified in nail patella syndrome (NPS) patients
J 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 collagen
I 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 children
J Adams, E I McIntosh, B L Weade
Cell Structure and Function
|
July 8, 2000
The pleiotropic effects of fibroblast growth factor receptors in mammalian development
I 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 patients
M 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 counselling
A 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 reaction
I McIntosh, J R Govan, D J Brock
Current Opinion in Genetics & Development
|
June 1, 1996
Bone dysplasias in man: molecular insights
C 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 UK
I McIntosh, M L Lorenzo, D J Brock
Page
of 10