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J M Connor

Showing results (71-80 of 181) with videos related to

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Journal of Medical Genetics|February 1, 1984
Concordant monozygotic twins with bilateral renal agenesisJ R Yates, G Mortimer, J M Connor, et al.
Human Genetics|January 1, 1989
Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndromeJ Galt, E Boyd, J M Connor, et al.
Human Genetics|April 1, 1992
Regional chromosomal assignment of the human platelet phosphofructokinase gene to 10p15N Morrison, C Simpson, L Fothergill-Gilmore, et al.
Prenatal Diagnosis|March 1, 1992
The psychosocial sequelae of a second-trimester termination of pregnancy for fetal abnormalityM C White-van Mourik, J M Connor, M A Ferguson-Smith
Human Mutation|January 1, 1994
A novel insertional mutation of a single base in exon 34 of the neurofibromatosis-1 geneS M Purandare, H R Davidson, W G Lanyon, et al.
Human Genetics|April 1, 1990
Regional assignment of the human C1-inhibitor gene to 11q11-q13.1A Theriault, K Whaley, A R McPhaden, et al.
Prenatal Diagnosis|June 1, 1992
Variation in the levels of pregnancy-specific beta-1-glycoprotein in maternal serum from chromosomally abnormal pregnanciesG W Graham, J A Crossley, D A Aitken, et al.
Prenatal Diagnosis|August 1, 1990
Patient care before and after termination of pregnancy for neural tube defectsM C White-Van Mourik, J M Connor, M A Ferguson-Smith
Molecular and Cellular Probes|April 1, 1996
A practical strategy for detection of major chromosome aneuploidies using ratio-mixing fluorescence in situ hybridizationS M Mohaddes, E Boyd, A Morris, et al.
Scottish Medical Journal|January 1, 1985
Pycnodysostosis in a Pakistani family: case presentation and reviewA M Kerr, M M Loudon, K M Goel, et al.
Pageof 19

Showing results (71-80 of 181) with videos related to

Sort By:
Pageof 19
Journal of Medical Genetics|February 1, 1984
Concordant monozygotic twins with bilateral renal agenesisJ R Yates, G Mortimer, J M Connor, et al.
Human Genetics|January 1, 1989
Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndromeJ Galt, E Boyd, J M Connor, et al.
Human Genetics|April 1, 1992
Regional chromosomal assignment of the human platelet phosphofructokinase gene to 10p15N Morrison, C Simpson, L Fothergill-Gilmore, et al.
Prenatal Diagnosis|March 1, 1992
The psychosocial sequelae of a second-trimester termination of pregnancy for fetal abnormalityM C White-van Mourik, J M Connor, M A Ferguson-Smith
Human Mutation|January 1, 1994
A novel insertional mutation of a single base in exon 34 of the neurofibromatosis-1 geneS M Purandare, H R Davidson, W G Lanyon, et al.
Human Genetics|April 1, 1990
Regional assignment of the human C1-inhibitor gene to 11q11-q13.1A Theriault, K Whaley, A R McPhaden, et al.
Prenatal Diagnosis|June 1, 1992
Variation in the levels of pregnancy-specific beta-1-glycoprotein in maternal serum from chromosomally abnormal pregnanciesG W Graham, J A Crossley, D A Aitken, et al.
Prenatal Diagnosis|August 1, 1990
Patient care before and after termination of pregnancy for neural tube defectsM C White-Van Mourik, J M Connor, M A Ferguson-Smith
Molecular and Cellular Probes|April 1, 1996
A practical strategy for detection of major chromosome aneuploidies using ratio-mixing fluorescence in situ hybridizationS M Mohaddes, E Boyd, A Morris, et al.
Scottish Medical Journal|January 1, 1985
Pycnodysostosis in a Pakistani family: case presentation and reviewA M Kerr, M M Loudon, K M Goel, et al.
Pageof 19