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M Pembrey

Showing results (31-40 of 48) with videos related to

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Journal of Medical Genetics|September 1, 1987
Congenital cutis laxa with retardation of growth and developmentM A Patton, J Tolmie, P Ruthnum, et al.
American Journal of Medical Genetics|May 15, 1993
Concordance and recessive inheritance of Leber congenital amaurosisS R Lambert, S Sherman, D Taylor, et al.
American Journal of Medical Genetics|October 1, 1988
Genetic prediction in X-linked agammaglobulinaemiaY L Lau, R J Levinsky, S Malcolm, et al.
European Journal of Human Genetics : EJHG|September 12, 2000
A new human genetic resource: a DNA bank established as part of the Avon longitudinal study of pregnancy and childhood (ALSPAC)R W Jones, S Ring, L Tyfield, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|July 9, 2002
An interaction between the IL-4Ralpha gene and infection is associated with atopic eczema in young childrenR E Callard, R Hamvas, C Chatterton, et al.
Human Molecular Genetics|August 1, 1994
Angelman syndrome associated with a maternal 15q11-13 deletion of less than 200 kbJ L Buxton, C T Chan, H Gilbert, et al.
Lancet (London, England)|March 15, 1986
Deletion on the X chromosome detected by direct DNA analysis in one of two unrelated boys with glycerol kinase deficiency, adrenal hypoplasia, and Duchenne muscular dystrophyD B Dunger, K E Davies, M Pembrey, et al.
Annals of Human Genetics|April 22, 2006
An investigation of FRAXA intermediate allele phenotype in a longitudinal sampleS Ennis, A Murray, S Youings, et al.
Journal of Thrombosis and Haemostasis : JTH|August 30, 2008
Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysisT Dudding, J Heron, A Thakkinstian, et al.
Nature Genetics|April 1, 1996
Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4B Coyle, R Coffey, J A Armour, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|September 1, 1987
Congenital cutis laxa with retardation of growth and developmentM A Patton, J Tolmie, P Ruthnum, et al.
American Journal of Medical Genetics|May 15, 1993
Concordance and recessive inheritance of Leber congenital amaurosisS R Lambert, S Sherman, D Taylor, et al.
American Journal of Medical Genetics|October 1, 1988
Genetic prediction in X-linked agammaglobulinaemiaY L Lau, R J Levinsky, S Malcolm, et al.
European Journal of Human Genetics : EJHG|September 12, 2000
A new human genetic resource: a DNA bank established as part of the Avon longitudinal study of pregnancy and childhood (ALSPAC)R W Jones, S Ring, L Tyfield, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|July 9, 2002
An interaction between the IL-4Ralpha gene and infection is associated with atopic eczema in young childrenR E Callard, R Hamvas, C Chatterton, et al.
Human Molecular Genetics|August 1, 1994
Angelman syndrome associated with a maternal 15q11-13 deletion of less than 200 kbJ L Buxton, C T Chan, H Gilbert, et al.
Lancet (London, England)|March 15, 1986
Deletion on the X chromosome detected by direct DNA analysis in one of two unrelated boys with glycerol kinase deficiency, adrenal hypoplasia, and Duchenne muscular dystrophyD B Dunger, K E Davies, M Pembrey, et al.
Annals of Human Genetics|April 22, 2006
An investigation of FRAXA intermediate allele phenotype in a longitudinal sampleS Ennis, A Murray, S Youings, et al.
Journal of Thrombosis and Haemostasis : JTH|August 30, 2008
Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysisT Dudding, J Heron, A Thakkinstian, et al.
Nature Genetics|April 1, 1996
Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4B Coyle, R Coffey, J A Armour, et al.
Pageof 5