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Liehr

Showing results (711-720 of 1,099) with videos related to

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Translational Neuroscience|January 27, 2017
Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the <i>DPYD</i> enigmaLukrecija Brečević, Martina Rinčić, Željka Krsnik, et al.
Hormones & Cancer|March 17, 2019
Role of Estrogen in Androgen-Induced Prostate Carcinogenesis in NBL RatsNur Ozten, Katherine Vega, Joachim Liehr, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16Heike Starke, Beate Mitulla, Angela Nietzel, et al.
Journal of Vascular and Interventional Radiology : JVIR|April 26, 2011
Prevention of intraprocedural puncture site bleeding during arterial port implantation by use of a suture-mediated arterial closure system: a prospective randomized trialOliver Dudeck, Skadi Wilhelmsen, Patrick Stübs, et al.
Genetic Counseling (Geneva, Switzerland)|October 23, 2010
Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouthS Balci, B Yuksel Konuk, F Atik, et al.
Prenatal Diagnosis|October 20, 2000
Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexingS Jakubiczka, B Mitulla, T Liehr, et al.
Critical Care Medicine|November 1, 2006
National evaluation of healthcare provider attitudes toward organ donation after cardiac deathM Susan Mandell, Stacy Zamudio, Debbie Seem, et al.
Chromosoma|April 16, 2016
Integrated gene mapping and synteny studies give insights into the evolution of a sex proto-chromosome in Solea senegalensisSilvia Portela-Bens, Manuel Alejandro Merlo, María Esther Rodríguez, et al.
Meta Gene|January 22, 2015
De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic featuresKonstantinos Varvagiannis, Ioannis Papoulidis, Theodora Koromila, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 18, 2025
Satellite DNA Amplification in Advanced Prostate Cancer Is Largely Independent From Euchromatic and Oncogene AmpliconsAnja Weise, Antonio Augusto Ornellas, Gilda Alves, et al.
Pageof 110

Showing results (711-720 of 1,099) with videos related to

Sort By:
Pageof 110
Translational Neuroscience|January 27, 2017
Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the <i>DPYD</i> enigmaLukrecija Brečević, Martina Rinčić, Željka Krsnik, et al.
Hormones & Cancer|March 17, 2019
Role of Estrogen in Androgen-Induced Prostate Carcinogenesis in NBL RatsNur Ozten, Katherine Vega, Joachim Liehr, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16Heike Starke, Beate Mitulla, Angela Nietzel, et al.
Journal of Vascular and Interventional Radiology : JVIR|April 26, 2011
Prevention of intraprocedural puncture site bleeding during arterial port implantation by use of a suture-mediated arterial closure system: a prospective randomized trialOliver Dudeck, Skadi Wilhelmsen, Patrick Stübs, et al.
Genetic Counseling (Geneva, Switzerland)|October 23, 2010
Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouthS Balci, B Yuksel Konuk, F Atik, et al.
Prenatal Diagnosis|October 20, 2000
Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexingS Jakubiczka, B Mitulla, T Liehr, et al.
Critical Care Medicine|November 1, 2006
National evaluation of healthcare provider attitudes toward organ donation after cardiac deathM Susan Mandell, Stacy Zamudio, Debbie Seem, et al.
Chromosoma|April 16, 2016
Integrated gene mapping and synteny studies give insights into the evolution of a sex proto-chromosome in Solea senegalensisSilvia Portela-Bens, Manuel Alejandro Merlo, María Esther Rodríguez, et al.
Meta Gene|January 22, 2015
De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic featuresKonstantinos Varvagiannis, Ioannis Papoulidis, Theodora Koromila, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 18, 2025
Satellite DNA Amplification in Advanced Prostate Cancer Is Largely Independent From Euchromatic and Oncogene AmpliconsAnja Weise, Antonio Augusto Ornellas, Gilda Alves, et al.
Pageof 110