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Liehr

Showing results (751-760 of 1,099) with videos related to

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Journal of Medical Case Reports|August 5, 2010
Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case reportJoaquín Fernández-Toral, Laura Rodríguez, Ana Plasencia, et al.
Journal of Addictions Nursing|March 14, 2014
Project SMART: an interdisciplinary collaboration to design and test a mentored health promotion program for school childrenMarianne T Marcus, Wendell C Taylor, Thomas Walker, et al.
Princess Takamatsu Symposia|January 1, 1991
Multistage prostate carcinogenesis: the role of hormonesM C Bosland, H C Dreef-Van Der Meulen, S Sukumar, et al.
Der Urologe. Ausg. A|October 23, 2012
[Placement of percutaneous nephrostomy by open magnetic resonance imaging: clinical results and current status in urology]M Porsch, J J Wendler, F Fischbach, et al.
Urologia Internationalis|April 19, 2016
Measurement of Procedure-Specific Irrigation-Fluid Absorption in Transurethral Therapy of Lower Urinary Tract Syndrome, Using Ethanolic Saline and Breath AlcometryMarkus Porsch, Paul Mittelstädt, Johann Jakob Wendler, et al.
Journal of Hepatology|March 26, 1998
Endoscopic sclerotherapy with fibrin glue as compared with polidocanol to prevent early esophageal variceal rebleedingT Zimmer, F Rucktäschel, U Stölzel, et al.
International Journal of Molecular Medicine|April 10, 2003
Evidence for a new microdeletion syndrome in 15q21T Liehr, H Starke, A Heller, et al.
Molecular Cytogenetics|March 17, 2009
Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardationBernd Auber, Verena Bruemmer, Barbara Zoll, et al.
Gene|December 17, 2013
A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotypeI Papoulidis, E Papageorgiou, E Siomou, et al.
Experimental and Therapeutic Medicine|March 27, 2014
Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literatureEmmanouil Manolakos, Annalisa Vetro, Antonios Garas, et al.
Pageof 110

Showing results (751-760 of 1,099) with videos related to

Sort By:
Pageof 110
Journal of Medical Case Reports|August 5, 2010
Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case reportJoaquín Fernández-Toral, Laura Rodríguez, Ana Plasencia, et al.
Journal of Addictions Nursing|March 14, 2014
Project SMART: an interdisciplinary collaboration to design and test a mentored health promotion program for school childrenMarianne T Marcus, Wendell C Taylor, Thomas Walker, et al.
Princess Takamatsu Symposia|January 1, 1991
Multistage prostate carcinogenesis: the role of hormonesM C Bosland, H C Dreef-Van Der Meulen, S Sukumar, et al.
Der Urologe. Ausg. A|October 23, 2012
[Placement of percutaneous nephrostomy by open magnetic resonance imaging: clinical results and current status in urology]M Porsch, J J Wendler, F Fischbach, et al.
Urologia Internationalis|April 19, 2016
Measurement of Procedure-Specific Irrigation-Fluid Absorption in Transurethral Therapy of Lower Urinary Tract Syndrome, Using Ethanolic Saline and Breath AlcometryMarkus Porsch, Paul Mittelstädt, Johann Jakob Wendler, et al.
Journal of Hepatology|March 26, 1998
Endoscopic sclerotherapy with fibrin glue as compared with polidocanol to prevent early esophageal variceal rebleedingT Zimmer, F Rucktäschel, U Stölzel, et al.
International Journal of Molecular Medicine|April 10, 2003
Evidence for a new microdeletion syndrome in 15q21T Liehr, H Starke, A Heller, et al.
Molecular Cytogenetics|March 17, 2009
Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardationBernd Auber, Verena Bruemmer, Barbara Zoll, et al.
Gene|December 17, 2013
A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotypeI Papoulidis, E Papageorgiou, E Siomou, et al.
Experimental and Therapeutic Medicine|March 27, 2014
Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literatureEmmanouil Manolakos, Annalisa Vetro, Antonios Garas, et al.
Pageof 110