J L Simpson|O P Phillips - JoVE Visualize

Showing results (91-100 of 235) with videos related to

Pageof 24

Sort By:

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 fetusesJ Zhao, A T Tharapel, L P Shulman, et al.

Human Genetics|November 1, 1992

Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesisE K Pivnick, S Wachtel, D Woods, et al.

American Journal of Obstetrics and Gynecology|February 15, 1979

Analysis for amniotic fluid crystallization in second-trimester amniocentesisS Elias, A O Martin, V A Patel, et al.

Birth Defects Original Article Series|May 1, 1971

Progressive idiopathic clitoral hypertrophy in a child: a previously undescribed type of female pseudohermaphroditismL S Gordon, G Morillo-Cucci, G Mulholland, et al.

Carcinogenesis|July 1, 1990

Cytokeratin expression during AFB1-induced carcinogenesisJ A Green, P Carthew, E Heuillet, et al.

Human Genetics|June 1, 1990

Failure to document fetal cells in maternal circulation using the Selypes-Lorencz "air-culture" cytogenetic techniqueM Youssef, L P Shulman, A T Tharapel, et al.

Acta Cytologica|May 1, 1997

Hodgkin's disease variant of Richter's syndrome. Report of a case with diagnosis by fine needle biopsyJ L Simpson, A T Moriarty, J Earls, et al.

American Journal of Obstetrics and Gynecology|March 1, 1996

Risk of fetal mosaicism when placental mosaicism is diagnosed by chorionic villus samplingO P Phillips, A T Tharapel, J L Lerner, et al.

Human Genetics|September 1, 1996

A jumping Robertsonian translocation: a molecular and cytogenetic studyS J Gross, A T Tharapel, O P Phillips, 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 villiM B Qumsiyeh, A T Tharapel, L P Shulman, et al.

Pageof 24

Showing results (91-100 of 235) with videos related to

Sort By:

Pageof 24

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 fetusesJ Zhao, A T Tharapel, L P Shulman, et al.

Human Genetics|November 1, 1992

Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesisE K Pivnick, S Wachtel, D Woods, et al.

American Journal of Obstetrics and Gynecology|February 15, 1979

Analysis for amniotic fluid crystallization in second-trimester amniocentesisS Elias, A O Martin, V A Patel, et al.

Birth Defects Original Article Series|May 1, 1971

Progressive idiopathic clitoral hypertrophy in a child: a previously undescribed type of female pseudohermaphroditismL S Gordon, G Morillo-Cucci, G Mulholland, et al.

Carcinogenesis|July 1, 1990

Cytokeratin expression during AFB1-induced carcinogenesisJ A Green, P Carthew, E Heuillet, et al.

Human Genetics|June 1, 1990

Failure to document fetal cells in maternal circulation using the Selypes-Lorencz "air-culture" cytogenetic techniqueM Youssef, L P Shulman, A T Tharapel, et al.

Acta Cytologica|May 1, 1997

Hodgkin's disease variant of Richter's syndrome. Report of a case with diagnosis by fine needle biopsyJ L Simpson, A T Moriarty, J Earls, et al.

American Journal of Obstetrics and Gynecology|March 1, 1996

Risk of fetal mosaicism when placental mosaicism is diagnosed by chorionic villus samplingO P Phillips, A T Tharapel, J L Lerner, et al.

Human Genetics|September 1, 1996

A jumping Robertsonian translocation: a molecular and cytogenetic studyS J Gross, A T Tharapel, O P Phillips, 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 villiM B Qumsiyeh, A T Tharapel, L P Shulman, et al.

Pageof 24