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J M Connor

Showing results (81-90 of 181) with videos related to

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American Journal of Medical Genetics|July 12, 1996
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardationA K Gedeon, I A Glass, J M Connor, et al.
The Journal of Bone and Joint Surgery. British Volume|January 1, 1988
Spondylothoracic and spondylocostal dysostosis. Hereditary forms of spinal deformityA P Roberts, A N Conner, J L Tolmie, et al.
Human Genetics|September 1, 1992
Detection of seven point mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria, by direct sequencing of in vitro amplified cDNAC S Mgone, W G Lanyon, M R Moore, et al.
Molecular and Cellular Probes|June 20, 1998
Acute intermittent porphyria: alternative splicing of hydroxymethylbilane synthase mRNA excludes exons 3 and 12P M Ong, W G Lanyon, M R Moore, et al.
Human Genetics|March 1, 1992
Regional chromosomal assignment of genes encoding the alpha and beta subunits of human complement protein C8 to 1p32A Theriault, E Boyd, K Whaley, et al.
Human Molecular Genetics|April 1, 1994
A novel splice donor mutation affecting position +3 in intron 6 of the factor VIII geneS I Bidichandani, C R Shiach, W G Lanyon, et al.
Birth Defects Original Article Series|January 1, 1992
The psychosocial sequelae of a second trimester termination of pregnancy for fetal abnormality over a two year periodM C White-Van Mourik, J M Connor, M A Ferguson-Smith
Archives of Disease in Childhood|September 1, 1985
Mucosal neuroma syndrome--a phenotype for malignancyM P White, K M Goel, J M Connor, et al.
Lancet (London, England)|June 25, 1994
Is genetic susceptibility for pre-eclampsia and eclampsia associated with implantation failure and fetal demise?R Arngrimsson, J M Connor, R T Geirsson, et al.
Human Genetics|June 1, 1994
Assignment of the gene encoding the human gonadotropin-releasing hormone receptor to 4q13.2-13.3 by fluorescence in situ hybridizationN Morrison, R E Sellar, E Boyd, et al.
Pageof 19

Showing results (81-90 of 181) with videos related to

Sort By:
Pageof 19
American Journal of Medical Genetics|July 12, 1996
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardationA K Gedeon, I A Glass, J M Connor, et al.
The Journal of Bone and Joint Surgery. British Volume|January 1, 1988
Spondylothoracic and spondylocostal dysostosis. Hereditary forms of spinal deformityA P Roberts, A N Conner, J L Tolmie, et al.
Human Genetics|September 1, 1992
Detection of seven point mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria, by direct sequencing of in vitro amplified cDNAC S Mgone, W G Lanyon, M R Moore, et al.
Molecular and Cellular Probes|June 20, 1998
Acute intermittent porphyria: alternative splicing of hydroxymethylbilane synthase mRNA excludes exons 3 and 12P M Ong, W G Lanyon, M R Moore, et al.
Human Genetics|March 1, 1992
Regional chromosomal assignment of genes encoding the alpha and beta subunits of human complement protein C8 to 1p32A Theriault, E Boyd, K Whaley, et al.
Human Molecular Genetics|April 1, 1994
A novel splice donor mutation affecting position +3 in intron 6 of the factor VIII geneS I Bidichandani, C R Shiach, W G Lanyon, et al.
Birth Defects Original Article Series|January 1, 1992
The psychosocial sequelae of a second trimester termination of pregnancy for fetal abnormality over a two year periodM C White-Van Mourik, J M Connor, M A Ferguson-Smith
Archives of Disease in Childhood|September 1, 1985
Mucosal neuroma syndrome--a phenotype for malignancyM P White, K M Goel, J M Connor, et al.
Lancet (London, England)|June 25, 1994
Is genetic susceptibility for pre-eclampsia and eclampsia associated with implantation failure and fetal demise?R Arngrimsson, J M Connor, R T Geirsson, et al.
Human Genetics|June 1, 1994
Assignment of the gene encoding the human gonadotropin-releasing hormone receptor to 4q13.2-13.3 by fluorescence in situ hybridizationN Morrison, R E Sellar, E Boyd, et al.
Pageof 19