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Prenatal Diagnosis
|
February 1, 1997
Discordant direct and culture results following chorionic villus sampling and the diagnosis of a third cell line in the fetus
O P Phillips, G V Velagaleti, A T Tharapel, et al.
American Journal of Medical Genetics
|
August 8, 1997
Rapid identification of marker chromosomes using primed in situ labeling (PRINS)
G V Velagaleti, S A Tharapel, P R Martens, et al.
Journal of Medical Genetics
|
August 1, 1986
Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13
S A Tharapel, R C Lewandowski, A T Tharapel, et al.
Cancer Genetics and Cytogenetics
|
March 15, 1986
Philadelphia chromosome-positive chronic myelocytic leukemia with a supplementary t(4;9)(q21;p22) and long survival
S A Tharapel, G I Plitman, A T Tharapel, et al.
Annales De Genetique
|
August 26, 1998
Prenatal karyotyping using fetal blood obtained by cordocentesis: rapid and accurate results within 24 hours
S A Tharapel, V G Dev, L P Shulman, et al.
American Journal of Medical Genetics
|
October 1, 1991
High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangement
M B Qumsiyeh, R S Wilroy, J N Peeden, et al.
Journal of the Society for Gynecologic Investigation
|
April 1, 1994
Molecular analysis to assign parental origin and distinguish de novo i(21q) from t(21q21q) in two Down syndrome fetuses
J Zhao, A T Tharapel, L P Shulman, et al.
Human Genetics
|
June 1, 1990
Failure to document fetal cells in maternal circulation using the Selypes-Lorencz "air-culture" cytogenetic technique
M Youssef, L P Shulman, A T Tharapel, et al.
Fertility and Sterility
|
October 1, 1991
Segregation analysis and genetic counseling when both parents carry balanced chromosomal translocations
O P Phillips, A T Tharapel, L P Shulman, et al.
Journal of Medical Genetics
|
December 1, 1990
Anaphase lag as the most likely mechanism for monosomy X in direct cytotrophoblasts but not in mesenchymal core cells from the same villi
M B Qumsiyeh, A T Tharapel, L P Shulman, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 49) with videos related to
Sort By:
Page
of 5
Prenatal Diagnosis
|
February 1, 1997
Discordant direct and culture results following chorionic villus sampling and the diagnosis of a third cell line in the fetus
O P Phillips, G V Velagaleti, A T Tharapel, et al.
American Journal of Medical Genetics
|
August 8, 1997
Rapid identification of marker chromosomes using primed in situ labeling (PRINS)
G V Velagaleti, S A Tharapel, P R Martens, et al.
Journal of Medical Genetics
|
August 1, 1986
Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13
S A Tharapel, R C Lewandowski, A T Tharapel, et al.
Cancer Genetics and Cytogenetics
|
March 15, 1986
Philadelphia chromosome-positive chronic myelocytic leukemia with a supplementary t(4;9)(q21;p22) and long survival
S A Tharapel, G I Plitman, A T Tharapel, et al.
Annales De Genetique
|
August 26, 1998
Prenatal karyotyping using fetal blood obtained by cordocentesis: rapid and accurate results within 24 hours
S A Tharapel, V G Dev, L P Shulman, et al.
American Journal of Medical Genetics
|
October 1, 1991
High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangement
M B Qumsiyeh, R S Wilroy, J N Peeden, et al.
Journal of the Society for Gynecologic Investigation
|
April 1, 1994
Molecular analysis to assign parental origin and distinguish de novo i(21q) from t(21q21q) in two Down syndrome fetuses
J Zhao, A T Tharapel, L P Shulman, et al.
Human Genetics
|
June 1, 1990
Failure to document fetal cells in maternal circulation using the Selypes-Lorencz "air-culture" cytogenetic technique
M Youssef, L P Shulman, A T Tharapel, et al.
Fertility and Sterility
|
October 1, 1991
Segregation analysis and genetic counseling when both parents carry balanced chromosomal translocations
O P Phillips, A T Tharapel, L P Shulman, et al.
Journal of Medical Genetics
|
December 1, 1990
Anaphase lag as the most likely mechanism for monosomy X in direct cytotrophoblasts but not in mesenchymal core cells from the same villi
M B Qumsiyeh, A T Tharapel, L P Shulman, et al.
Page
of 5