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R Fitzpatrick

Showing results (471-480 of 555) with videos related to

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Human Molecular Genetics|December 24, 2013
Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequenceJacqueline K Rainger, Shipra Bhatia, Hemant Bengani, et al.
Antimicrobial Agents and Chemotherapy|July 14, 2001
GT160-246, a toxin binding polymer for treatment of Clostridium difficile colitisC B Kurtz, E P Cannon, A Brezzani, et al.
Journal of the American College of Cardiology|March 17, 2018
Cardiac Genetic Predisposition in Sudden Infant Death SyndromeDavid J Tester, Leonie C H Wong, Pritha Chanana, et al.
Blood Cancer Journal|August 20, 2013
Loss of the xeroderma pigmentosum group B protein binding site impairs p210 BCR/ABL1 leukemogenic activityN L Pannucci, D Li, S Sahay, et al.
Chemistry of Materials : a Publication of the American Chemical Society|March 6, 2023
Monitoring the Formation of Nickel-Poor and Nickel-Rich Oxide Cathode Materials for Lithium-Ion Batteries with Synchrotron RadiationBixian Ying, Jack R Fitzpatrick, Zhenjie Teng, et al.
American Journal of Medical Genetics. Part A|April 7, 2005
SOX2 anophthalmia syndromeNicola K Ragge, Birgit Lorenz, Adele Schneider, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Cornelia de Lange syndrome: extending the physical and psychological phenotypeChris Oliver, Maria Francesca Bedeschi, Natalie Blagowidow, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growthSally Ann Lynch, Nicola Foulds, Ann-Charlotte Thuresson, et al.
American Journal of Human Genetics|April 1, 2008
FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormalityJ A Fantes, E Boland, J Ramsay, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2018
Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disordersCaroline F Wright, Jeremy F McRae, Stephen Clayton, et al.
Pageof 56

Showing results (471-480 of 555) with videos related to

Sort By:
Pageof 56
Human Molecular Genetics|December 24, 2013
Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequenceJacqueline K Rainger, Shipra Bhatia, Hemant Bengani, et al.
Antimicrobial Agents and Chemotherapy|July 14, 2001
GT160-246, a toxin binding polymer for treatment of Clostridium difficile colitisC B Kurtz, E P Cannon, A Brezzani, et al.
Journal of the American College of Cardiology|March 17, 2018
Cardiac Genetic Predisposition in Sudden Infant Death SyndromeDavid J Tester, Leonie C H Wong, Pritha Chanana, et al.
Blood Cancer Journal|August 20, 2013
Loss of the xeroderma pigmentosum group B protein binding site impairs p210 BCR/ABL1 leukemogenic activityN L Pannucci, D Li, S Sahay, et al.
Chemistry of Materials : a Publication of the American Chemical Society|March 6, 2023
Monitoring the Formation of Nickel-Poor and Nickel-Rich Oxide Cathode Materials for Lithium-Ion Batteries with Synchrotron RadiationBixian Ying, Jack R Fitzpatrick, Zhenjie Teng, et al.
American Journal of Medical Genetics. Part A|April 7, 2005
SOX2 anophthalmia syndromeNicola K Ragge, Birgit Lorenz, Adele Schneider, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Cornelia de Lange syndrome: extending the physical and psychological phenotypeChris Oliver, Maria Francesca Bedeschi, Natalie Blagowidow, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growthSally Ann Lynch, Nicola Foulds, Ann-Charlotte Thuresson, et al.
American Journal of Human Genetics|April 1, 2008
FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormalityJ A Fantes, E Boland, J Ramsay, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2018
Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disordersCaroline F Wright, Jeremy F McRae, Stephen Clayton, et al.
Pageof 56