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A T Tharapel

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Human Genetics|October 1, 1991
Sister chromatid exchange (SCE) frequencies differ between directly prepared cytotrophoblasts and cultured mesenchymal core cellsL P Shulman, L R Li, A T Tharapel, et al.
American Journal of Obstetrics and Gynecology|December 1, 1989
Rapid chromosome analysis with the use of spontaneously dividing cells derived from umbilical cord blood (fetal and neonatal)R E Tipton, A T Tharapel, H H Chang, et al.
Journal of Medical Genetics|August 1, 1990
Partial duplication of the long arm of chromosome 6: a clinically recognisable syndromeE K Pivnick, M B Qumsiyeh, A T Tharapel, et al.
Annales De Genetique|January 1, 1983
Diploid-triploid mosaicism: delineation of the syndromeA T Tharapel, R S Wilroy, P R Martens, et al.
Journal of Medical Genetics|May 1, 1993
Elucidation of the centromere involvement in an inversion (13) by fluorescent in situ hybridisationP L Gordon, J D Dalton, P R Martens, et al.
Prenatal Diagnosis|March 4, 2000
Fetal 'space-suit' hydrops in the first trimester: differentiating risk for chromosome abnormalities by delineating characteristics of nuchal translucencyL P Shulman, O P Phillips, D S Emerson, et al.
American Journal of Medical Genetics|January 1, 1992
Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndromeM B Qumsiyeh, J D Dalton, P L Gordon, et al.
American Journal of Obstetrics and Gynecology|July 14, 1998
Primed in situ labeling for rapid prenatal diagnosisG V Velagelati, L P Shulman, O P Phillips, et al.
American Journal of Medical Genetics|March 1, 1992
Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probesS A Tharapel, R S Wilroy, A M Keath, et al.
Prenatal Diagnosis|July 1, 1989
Resorbed co-twin as an explanation for discrepant chorionic villus results: non-mosaic 47,XX,+16 in villi (direct and culture) with normal (46,XX) amniotic fluid and neonatal bloodA T Tharapel, S Elias, L P Shulman, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Human Genetics|October 1, 1991
Sister chromatid exchange (SCE) frequencies differ between directly prepared cytotrophoblasts and cultured mesenchymal core cellsL P Shulman, L R Li, A T Tharapel, et al.
American Journal of Obstetrics and Gynecology|December 1, 1989
Rapid chromosome analysis with the use of spontaneously dividing cells derived from umbilical cord blood (fetal and neonatal)R E Tipton, A T Tharapel, H H Chang, et al.
Journal of Medical Genetics|August 1, 1990
Partial duplication of the long arm of chromosome 6: a clinically recognisable syndromeE K Pivnick, M B Qumsiyeh, A T Tharapel, et al.
Annales De Genetique|January 1, 1983
Diploid-triploid mosaicism: delineation of the syndromeA T Tharapel, R S Wilroy, P R Martens, et al.
Journal of Medical Genetics|May 1, 1993
Elucidation of the centromere involvement in an inversion (13) by fluorescent in situ hybridisationP L Gordon, J D Dalton, P R Martens, et al.
Prenatal Diagnosis|March 4, 2000
Fetal 'space-suit' hydrops in the first trimester: differentiating risk for chromosome abnormalities by delineating characteristics of nuchal translucencyL P Shulman, O P Phillips, D S Emerson, et al.
American Journal of Medical Genetics|January 1, 1992
Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndromeM B Qumsiyeh, J D Dalton, P L Gordon, et al.
American Journal of Obstetrics and Gynecology|July 14, 1998
Primed in situ labeling for rapid prenatal diagnosisG V Velagelati, L P Shulman, O P Phillips, et al.
American Journal of Medical Genetics|March 1, 1992
Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probesS A Tharapel, R S Wilroy, A M Keath, et al.
Prenatal Diagnosis|July 1, 1989
Resorbed co-twin as an explanation for discrepant chorionic villus results: non-mosaic 47,XX,+16 in villi (direct and culture) with normal (46,XX) amniotic fluid and neonatal bloodA T Tharapel, S Elias, L P Shulman, et al.
Pageof 5