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Philip A I Guthrie

Showing results (1-10 of 13) with videos related to

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Human Mutation|January 16, 2010
An expectation-maximization program for determining allelic spectrum from CNV data (CoNVEM): insights into population allelic architecture and its mutational historyTom R Gaunt, Santiago Rodriguez, Philip A I Guthrie, et al.
Gene|March 22, 2012
Complexity of a complex trait locus: HP, HPR, haemoglobin and cholesterolPhilip A I Guthrie, Santiago Rodriguez, Tom R Gaunt, et al.
Clinical Chemistry|April 29, 2006
Integrated single-label liquid-phase assay of APOE codons 112 and 158 and a lipoprotein study in British womenMohammad Reza Abdollahi, Philip A I Guthrie, George Davey Smith, et al.
Nucleic Acids Research|February 9, 2011
Amplification ratio control system for copy number variation genotypingPhilip A I Guthrie, Tom R Gaunt, Mohammed R Abdollahi, et al.
Biological Psychiatry|January 11, 2011
IQ, educational attainment, memory and plasma lipids: associations with apolipoprotein E genotype in 5995 childrenAmy E Taylor, Philip A I Guthrie, George Davey Smith, et al.
Annals of Human Genetics|May 22, 2012
Molecular and population analysis of natural selection on the human haptoglobin duplicationSantiago Rodriguez, Dylan M Williams, Philip A I Guthrie, et al.
Disease Markers|December 20, 2014
Haptoglobin duplicon, hemoglobin, and vitamin C: analyses in the british women's heart and health study and Caerphilly prospective studyPhilip A I Guthrie, Mohammad R Abdollahi, Tom Gaunt, et al.
Mitochondrion|August 19, 2017
Cardiometabolic phenotypes and mitochondrial DNA copy number in two cohorts of UK womenAnna L Guyatt, Kimberley Burrows, Philip A I Guthrie, et al.
Annals of Human Genetics|March 6, 2012
From a single whole exome read to notions of clinical screening: primary ciliary dyskinesia and RSPH9 p.Lys268del in the Arabian PeninsulaMuslim M Alsaadi, Tom R Gaunt, Christopher R Boustred, et al.
Human Mutation|September 17, 2014
Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesiaMuslim M Alsaadi, A Mesut Erzurumluoglu, Santiago Rodriguez, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Human Mutation|January 16, 2010
An expectation-maximization program for determining allelic spectrum from CNV data (CoNVEM): insights into population allelic architecture and its mutational historyTom R Gaunt, Santiago Rodriguez, Philip A I Guthrie, et al.
Gene|March 22, 2012
Complexity of a complex trait locus: HP, HPR, haemoglobin and cholesterolPhilip A I Guthrie, Santiago Rodriguez, Tom R Gaunt, et al.
Clinical Chemistry|April 29, 2006
Integrated single-label liquid-phase assay of APOE codons 112 and 158 and a lipoprotein study in British womenMohammad Reza Abdollahi, Philip A I Guthrie, George Davey Smith, et al.
Nucleic Acids Research|February 9, 2011
Amplification ratio control system for copy number variation genotypingPhilip A I Guthrie, Tom R Gaunt, Mohammed R Abdollahi, et al.
Biological Psychiatry|January 11, 2011
IQ, educational attainment, memory and plasma lipids: associations with apolipoprotein E genotype in 5995 childrenAmy E Taylor, Philip A I Guthrie, George Davey Smith, et al.
Annals of Human Genetics|May 22, 2012
Molecular and population analysis of natural selection on the human haptoglobin duplicationSantiago Rodriguez, Dylan M Williams, Philip A I Guthrie, et al.
Disease Markers|December 20, 2014
Haptoglobin duplicon, hemoglobin, and vitamin C: analyses in the british women's heart and health study and Caerphilly prospective studyPhilip A I Guthrie, Mohammad R Abdollahi, Tom Gaunt, et al.
Mitochondrion|August 19, 2017
Cardiometabolic phenotypes and mitochondrial DNA copy number in two cohorts of UK womenAnna L Guyatt, Kimberley Burrows, Philip A I Guthrie, et al.
Annals of Human Genetics|March 6, 2012
From a single whole exome read to notions of clinical screening: primary ciliary dyskinesia and RSPH9 p.Lys268del in the Arabian PeninsulaMuslim M Alsaadi, Tom R Gaunt, Christopher R Boustred, et al.
Human Mutation|September 17, 2014
Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesiaMuslim M Alsaadi, A Mesut Erzurumluoglu, Santiago Rodriguez, et al.
Pageof 2