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J M Connor

Showing results (111-120 of 181) with videos related to

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Human Genetics|December 1, 1993
Detection of a high mutation frequency in exon 12 of the porphobilinogen deaminase gene in patients with acute intermittent porphyriaC S Mgone, W G Lanyon, M R Moore, et al.
Journal of Animal Science|February 25, 2003
Fenceline contact of beef calves with their dams at weaning reduces the negative effects of separation on behavior and growth rateE O Price, J E Harris, R E Borgward, et al.
Archives of Dermatology|March 23, 1999
Genetic and environmental influences in the development of multiple primary melanomaA D Burden, J Newell, N Andrew, et al.
Human Molecular Genetics|May 1, 1994
Identification of five novel mutations in the porphobilinogen deaminase geneC S Mgone, W G Lanyon, M R Moore, et al.
Human Genetics|June 1, 1991
Chromosomal assignment of a large tRNA gene cluster (tRNA(Leu), tRNA(Gln), tRNA(Lys), tRNA(Arg), tRNA(Gly)) to 17p13.1N Morrison, J P Goddard, D H Ledbetter, et al.
Human Genetics|May 1, 1995
Detection of mutations in ectopic factor VIII transcripts from nine haemophilia A patients and the correlation with phenotypeS I Bidichandani, W G Lanyon, C R Shiach, et al.
Prenatal Diagnosis|March 29, 2002
Maternal smoking: age distribution, levels of alpha-fetoprotein and human chorionic gonadotrophin, and effect on detection of Down syndrome pregnancies in second-trimester screeningJ A Crossley, D A Aitken, S M L Waugh, et al.
Prenatal Diagnosis|February 1, 1987
Second trimester prenatal diagnosis of the Jarcho-Levin syndromeJ L Tolmie, M J Whittle, M B McNay, et al.
Journal of Medical Genetics|August 25, 2005
Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twinsD Johnson, N Morrison, L Grant, et al.
Cancer Genetics and Cytogenetics|April 13, 1999
Detection of t(12;21) in childhood acute lymphoblastic leukemia by fluorescence in situ hybridizationD H Spathas, J Stewart, I O Singer, et al.
Pageof 19

Showing results (111-120 of 181) with videos related to

Sort By:
Pageof 19
Human Genetics|December 1, 1993
Detection of a high mutation frequency in exon 12 of the porphobilinogen deaminase gene in patients with acute intermittent porphyriaC S Mgone, W G Lanyon, M R Moore, et al.
Journal of Animal Science|February 25, 2003
Fenceline contact of beef calves with their dams at weaning reduces the negative effects of separation on behavior and growth rateE O Price, J E Harris, R E Borgward, et al.
Archives of Dermatology|March 23, 1999
Genetic and environmental influences in the development of multiple primary melanomaA D Burden, J Newell, N Andrew, et al.
Human Molecular Genetics|May 1, 1994
Identification of five novel mutations in the porphobilinogen deaminase geneC S Mgone, W G Lanyon, M R Moore, et al.
Human Genetics|June 1, 1991
Chromosomal assignment of a large tRNA gene cluster (tRNA(Leu), tRNA(Gln), tRNA(Lys), tRNA(Arg), tRNA(Gly)) to 17p13.1N Morrison, J P Goddard, D H Ledbetter, et al.
Human Genetics|May 1, 1995
Detection of mutations in ectopic factor VIII transcripts from nine haemophilia A patients and the correlation with phenotypeS I Bidichandani, W G Lanyon, C R Shiach, et al.
Prenatal Diagnosis|March 29, 2002
Maternal smoking: age distribution, levels of alpha-fetoprotein and human chorionic gonadotrophin, and effect on detection of Down syndrome pregnancies in second-trimester screeningJ A Crossley, D A Aitken, S M L Waugh, et al.
Prenatal Diagnosis|February 1, 1987
Second trimester prenatal diagnosis of the Jarcho-Levin syndromeJ L Tolmie, M J Whittle, M B McNay, et al.
Journal of Medical Genetics|August 25, 2005
Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twinsD Johnson, N Morrison, L Grant, et al.
Cancer Genetics and Cytogenetics|April 13, 1999
Detection of t(12;21) in childhood acute lymphoblastic leukemia by fluorescence in situ hybridizationD H Spathas, J Stewart, I O Singer, et al.
Pageof 19