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Fertility and Sterility
|
December 20, 2000
46,XY monozygotic twins with discordant sex phenotype
S G Somkuti, S S Wachtel, J S Schinfeld, et al.
American Journal of Medical Genetics
|
September 1, 1990
Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2
E K Pivnick, R S Wilroy, J B Summitt, et al.
Annales De Genetique
|
May 20, 2000
Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicism
Y Tunca, R S Wilroy, J S Kadandale, et al.
American Journal of Obstetrics and Gynecology
|
November 1, 1990
Direct analysis of uncultured cytotrophoblastic cells from second- and third-trimester placentas: an accurate and rapid method for detection of fetal chromosome abnormalities
L P Shulman, A T Tharapel, C M Meyers, et al.
American Journal of Medical Genetics
|
November 14, 2000
Localization of SRY by primed in situ labeling in XX and XY sex reversal
J S Kadandale, S S Wachtel, Y Tunca, et al.
American Journal of Obstetrics and Gynecology
|
December 1, 1991
Sister chromatid exchange frequency in directly prepared cytotrophoblasts: demonstration of in vivo deoxyribonucleic acid damage in pregnant women who smoke cigarettes
L P Shulman, S Elias, A T Tharapel, et al.
Human Genetics
|
September 1, 1996
A jumping Robertsonian translocation: a molecular and cytogenetic study
S J Gross, A T Tharapel, O P Phillips, et al.
American Journal of Obstetrics and Gynecology
|
March 1, 1996
Risk of fetal mosaicism when placental mosaicism is diagnosed by chorionic villus sampling
O P Phillips, A T Tharapel, J L Lerner, et al.
American Journal of Human Genetics
|
March 1, 1993
Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions
A T Tharapel, K P Anderson, J L Simpson, et al.
Journal of Medical Genetics
|
September 1, 1996
Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases
E K Pivnick, G V Velagaleti, R S Wilroy, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 49) with videos related to
Sort By:
Page
of 5
Fertility and Sterility
|
December 20, 2000
46,XY monozygotic twins with discordant sex phenotype
S G Somkuti, S S Wachtel, J S Schinfeld, et al.
American Journal of Medical Genetics
|
September 1, 1990
Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2
E K Pivnick, R S Wilroy, J B Summitt, et al.
Annales De Genetique
|
May 20, 2000
Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicism
Y Tunca, R S Wilroy, J S Kadandale, et al.
American Journal of Obstetrics and Gynecology
|
November 1, 1990
Direct analysis of uncultured cytotrophoblastic cells from second- and third-trimester placentas: an accurate and rapid method for detection of fetal chromosome abnormalities
L P Shulman, A T Tharapel, C M Meyers, et al.
American Journal of Medical Genetics
|
November 14, 2000
Localization of SRY by primed in situ labeling in XX and XY sex reversal
J S Kadandale, S S Wachtel, Y Tunca, et al.
American Journal of Obstetrics and Gynecology
|
December 1, 1991
Sister chromatid exchange frequency in directly prepared cytotrophoblasts: demonstration of in vivo deoxyribonucleic acid damage in pregnant women who smoke cigarettes
L P Shulman, S Elias, A T Tharapel, et al.
Human Genetics
|
September 1, 1996
A jumping Robertsonian translocation: a molecular and cytogenetic study
S J Gross, A T Tharapel, O P Phillips, et al.
American Journal of Obstetrics and Gynecology
|
March 1, 1996
Risk of fetal mosaicism when placental mosaicism is diagnosed by chorionic villus sampling
O P Phillips, A T Tharapel, J L Lerner, et al.
American Journal of Human Genetics
|
March 1, 1993
Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions
A T Tharapel, K P Anderson, J L Simpson, et al.
Journal of Medical Genetics
|
September 1, 1996
Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases
E K Pivnick, G V Velagaleti, R S Wilroy, et al.
Page
of 5