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R Kadir

Showing results (11-20 of 17) with videos related to

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Clinical Genetics|July 25, 2018
Novel SBF1 splice-site null mutation broadens the clinical spectrum of Charcot-Marie-Tooth type 4B3 diseaseH Flusser, D Halperin, R Kadir, et al.
British Journal of Obstetrics and Gynaecology|January 27, 1998
First trimester sonographic detection of chromosomal abnormalities in an unselected populationD L Economides, B J Whitlow, R Kadir, et al.
The Malaysian Journal of Pathology|December 26, 2008
Fine needle aspiration cytology of neuroendocrine carcinoma of the breast--a case report and review of literatureAbdul A R Kadir, Krishnan R Iyengar, Suat Cheng Peh, et al.
Fetal Diagnosis and Therapy|October 10, 2009
Pentasomy 49,XXXXY diagnosed in utero: case report and systematic review of antenatal findingsP Peitsidis, E Manolakos, A Peitsidou, et al.
RSC Advances|May 2, 2022
Revisiting the seed-assisted synthesis of zeolites without organic structure-directing agents: insights from the CHA caseGrandprix T M Kadja, Iftitah R Kadir, Adroit T N Fajar, et al.
Elife|June 30, 2021
Nanoscape, a data-driven 3D real-time interactive virtual cell environmentShereen R Kadir, Andrew Lilja, Nick Gunn, et al.
Nature Communications|October 27, 2021
CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and miceD Halperin, A Stavsky, R Kadir, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Clinical Genetics|July 25, 2018
Novel SBF1 splice-site null mutation broadens the clinical spectrum of Charcot-Marie-Tooth type 4B3 diseaseH Flusser, D Halperin, R Kadir, et al.
British Journal of Obstetrics and Gynaecology|January 27, 1998
First trimester sonographic detection of chromosomal abnormalities in an unselected populationD L Economides, B J Whitlow, R Kadir, et al.
The Malaysian Journal of Pathology|December 26, 2008
Fine needle aspiration cytology of neuroendocrine carcinoma of the breast--a case report and review of literatureAbdul A R Kadir, Krishnan R Iyengar, Suat Cheng Peh, et al.
Fetal Diagnosis and Therapy|October 10, 2009
Pentasomy 49,XXXXY diagnosed in utero: case report and systematic review of antenatal findingsP Peitsidis, E Manolakos, A Peitsidou, et al.
RSC Advances|May 2, 2022
Revisiting the seed-assisted synthesis of zeolites without organic structure-directing agents: insights from the CHA caseGrandprix T M Kadja, Iftitah R Kadir, Adroit T N Fajar, et al.
Elife|June 30, 2021
Nanoscape, a data-driven 3D real-time interactive virtual cell environmentShereen R Kadir, Andrew Lilja, Nick Gunn, et al.
Nature Communications|October 27, 2021
CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and miceD Halperin, A Stavsky, R Kadir, et al.
Pageof 2