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M E Pembrey

Showing results (71-80 of 99) with videos related to

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Human Genetics|December 1, 1990
The major cystic fibrosis mutation in a British populationC J McMahon, S A Genet, H R Middleton-Price, et al.
Journal of Medical Genetics|December 1, 1992
Angelman syndrome with a chromosomal inversion 15 inv(p11q13) accompanied by a deletion in 15q11q13T Webb, J Clayton-Smith, X J Cheng, et al.
Journal of Medical Genetics|November 1, 1993
Molecular mechanisms in Angelman syndrome: a survey of 93 patientsC T Chan, J Clayton-Smith, X J Cheng, et al.
Archives of Disease in Childhood|March 1, 1984
Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophyM E Pembrey, K E Davies, R M Winter, et al.
Genomics|December 1, 1991
A multipedigree linkage study of X-linked deafness: linkage to Xq13-q21 and evidence for genetic heterogeneityW Reardon, H R Middleton-Price, L Sandkuijl, et al.
Human Genetics|March 1, 1987
Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletionS V Hodgson, M E Robertson, C N Fear, et al.
Journal of Medical Genetics|October 1, 1991
The non-deletion type of alpha thalassaemia/mental retardation: a recognisable dysmorphic syndrome with X linked inheritanceA O Wilkie, M E Pembrey, R J Gibbons, et al.
American Journal of Medical Genetics|May 1, 1988
Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysisA Hanauer, Y Alembik, S Gilgenkrantz, et al.
Lancet (London, England)|December 5, 1992
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNAW Reardon, R J Ross, M G Sweeney, et al.
Lancet (London, England)|March 23, 1991
Uniparental paternal disomy in Angelman's syndromeS Malcolm, J Clayton-Smith, M Nichols, et al.
Pageof 10

Showing results (71-80 of 99) with videos related to

Sort By:
Pageof 10
Human Genetics|December 1, 1990
The major cystic fibrosis mutation in a British populationC J McMahon, S A Genet, H R Middleton-Price, et al.
Journal of Medical Genetics|December 1, 1992
Angelman syndrome with a chromosomal inversion 15 inv(p11q13) accompanied by a deletion in 15q11q13T Webb, J Clayton-Smith, X J Cheng, et al.
Journal of Medical Genetics|November 1, 1993
Molecular mechanisms in Angelman syndrome: a survey of 93 patientsC T Chan, J Clayton-Smith, X J Cheng, et al.
Archives of Disease in Childhood|March 1, 1984
Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophyM E Pembrey, K E Davies, R M Winter, et al.
Genomics|December 1, 1991
A multipedigree linkage study of X-linked deafness: linkage to Xq13-q21 and evidence for genetic heterogeneityW Reardon, H R Middleton-Price, L Sandkuijl, et al.
Human Genetics|March 1, 1987
Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletionS V Hodgson, M E Robertson, C N Fear, et al.
Journal of Medical Genetics|October 1, 1991
The non-deletion type of alpha thalassaemia/mental retardation: a recognisable dysmorphic syndrome with X linked inheritanceA O Wilkie, M E Pembrey, R J Gibbons, et al.
American Journal of Medical Genetics|May 1, 1988
Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysisA Hanauer, Y Alembik, S Gilgenkrantz, et al.
Lancet (London, England)|December 5, 1992
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNAW Reardon, R J Ross, M G Sweeney, et al.
Lancet (London, England)|March 23, 1991
Uniparental paternal disomy in Angelman's syndromeS Malcolm, J Clayton-Smith, M Nichols, et al.
Pageof 10