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G Weber

Showing results (1151-1160 of 1,377) with videos related to

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Physical Review Letters|September 26, 2012
Polarization transfer of bremsstrahlung arising from spin-polarized electronsR Märtin, G Weber, R Barday, et al.
Leukemia|March 27, 2009
Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter studyA M Willasch, B Gruhn, T Coliva, et al.
Human Genetics|September 1, 1997
Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)S A Forbes, A A Pannett, J H Bassett, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|July 29, 2009
European Hernia Society guidelines on the treatment of inguinal hernia in adult patientsM P Simons, T Aufenacker, M Bay-Nielsen, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|September 26, 2012
Distribution of fluconazole-resistant Candida bloodstream isolates among hospitals and inpatient services in IsraelR Ben-Ami, G Rahav, H Elinav, et al.
European Journal of Human Genetics : EJHG|October 17, 2024
Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tractEsra Kesdiren, Helge Martens, Frank Brand, et al.
Brain : a Journal of Neurology|January 8, 2019
Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disabilityYuanyuan Liu, Julian Schubert, Lukas Sonnenberg, et al.
Human Molecular Genetics|March 24, 2017
Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformationsAnne Kosfeld, Frank Brand, Anna-Carina Weiss, et al.
Journal of Intellectual Disability Research : JIDR|July 6, 2011
The impact of living arrangements and deinstitutionalisation in the health status of persons with intellectual disability in EuropeR Martínez-Leal, L Salvador-Carulla, C Linehan, et al.
American Journal of Medical Genetics. Part A|February 28, 2012
A phenotype map for 14q32.3 terminal deletionsHartmut Engels, Herdit M Schüler, Alexander M Zink, et al.
Pageof 138

Showing results (1151-1160 of 1,377) with videos related to

Sort By:
Pageof 138
Physical Review Letters|September 26, 2012
Polarization transfer of bremsstrahlung arising from spin-polarized electronsR Märtin, G Weber, R Barday, et al.
Leukemia|March 27, 2009
Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter studyA M Willasch, B Gruhn, T Coliva, et al.
Human Genetics|September 1, 1997
Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)S A Forbes, A A Pannett, J H Bassett, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|July 29, 2009
European Hernia Society guidelines on the treatment of inguinal hernia in adult patientsM P Simons, T Aufenacker, M Bay-Nielsen, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|September 26, 2012
Distribution of fluconazole-resistant Candida bloodstream isolates among hospitals and inpatient services in IsraelR Ben-Ami, G Rahav, H Elinav, et al.
European Journal of Human Genetics : EJHG|October 17, 2024
Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tractEsra Kesdiren, Helge Martens, Frank Brand, et al.
Brain : a Journal of Neurology|January 8, 2019
Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disabilityYuanyuan Liu, Julian Schubert, Lukas Sonnenberg, et al.
Human Molecular Genetics|March 24, 2017
Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformationsAnne Kosfeld, Frank Brand, Anna-Carina Weiss, et al.
Journal of Intellectual Disability Research : JIDR|July 6, 2011
The impact of living arrangements and deinstitutionalisation in the health status of persons with intellectual disability in EuropeR Martínez-Leal, L Salvador-Carulla, C Linehan, et al.
American Journal of Medical Genetics. Part A|February 28, 2012
A phenotype map for 14q32.3 terminal deletionsHartmut Engels, Herdit M Schüler, Alexander M Zink, et al.
Pageof 138