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A T Tharapel

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Clinical Genetics|June 1, 1986
First trimester chorionic villi sampling and direct chromosome preparationsA T Tharapel, J V Dacus, S A Tharapel, et al.
American Journal of Medical Genetics|July 11, 1991
Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probesA T Tharapel, M B Qumsiyeh, P R Martens, et al.
American Journal of Medical Genetics|May 2, 1997
Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysisS Rajangam, R C Michaelis, G V Velagaleti, et al.
American Journal of Medical Genetics|May 8, 1995
Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridizationJ Zhao, P L Gordon, R S Wilroy, et al.
Fetal Diagnosis and Therapy|March 1, 1993
Inability to detect fetal metaphases in flow-sorted lymphocyte cultures based on maternal-fetal HLA differencesA T Tharapel, V L Jaswaney, M E Dockter, et al.
American Journal of Medical Genetics|March 21, 1998
Most Jacobsen syndrome deletion breakpoints occur distal to FRA11BR C Michaelis, G V Velagaleti, C Jones, et al.
Cytogenetics and Cell Genetics|August 18, 1999
Chromosome duplications and deletions and their mechanisms of originA T Tharapel, R C Michaelis, G V Velagaleti, et al.
American Journal of Perinatology|July 1, 1990
Diagnosis of trisomy 18 using spontaneously dividing cells from fetal umbilical cord blood: a novel approach for rapid late second and third trimester prenatal diagnosisA T Tharapel, M L Moretti, C M Meyers, et al.
American Journal of Perinatology|January 1, 1993
Mode of ascertainment is critical in assessing safety of percutaneous umbilical blood samplingL P Shulman, M L Moretti, A T Tharapel, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Clinical Genetics|June 1, 1986
First trimester chorionic villi sampling and direct chromosome preparationsA T Tharapel, J V Dacus, S A Tharapel, et al.
American Journal of Medical Genetics|July 11, 1991
Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probesA T Tharapel, M B Qumsiyeh, P R Martens, et al.
American Journal of Medical Genetics|May 2, 1997
Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysisS Rajangam, R C Michaelis, G V Velagaleti, et al.
American Journal of Medical Genetics|May 8, 1995
Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridizationJ Zhao, P L Gordon, R S Wilroy, et al.
Fetal Diagnosis and Therapy|March 1, 1993
Inability to detect fetal metaphases in flow-sorted lymphocyte cultures based on maternal-fetal HLA differencesA T Tharapel, V L Jaswaney, M E Dockter, et al.
American Journal of Medical Genetics|March 21, 1998
Most Jacobsen syndrome deletion breakpoints occur distal to FRA11BR C Michaelis, G V Velagaleti, C Jones, et al.
Cytogenetics and Cell Genetics|August 18, 1999
Chromosome duplications and deletions and their mechanisms of originA T Tharapel, R C Michaelis, G V Velagaleti, et al.
American Journal of Perinatology|July 1, 1990
Diagnosis of trisomy 18 using spontaneously dividing cells from fetal umbilical cord blood: a novel approach for rapid late second and third trimester prenatal diagnosisA T Tharapel, M L Moretti, C M Meyers, et al.
American Journal of Perinatology|January 1, 1993
Mode of ascertainment is critical in assessing safety of percutaneous umbilical blood samplingL P Shulman, M L Moretti, A T Tharapel, et al.
Pageof 5