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Showing results (161-170 of 174) with videos related to

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Neuroimage|June 6, 2009
Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individualsV Markov, A Krug, S Krach, et al.
Neurology|March 26, 2003
Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathyS Rudnik-Schöneborn, H H Goebel, W Schlote, et al.
Clinical Genetics|May 14, 2016
NSD1 duplication in Silver-Russell syndrome (SRS): molecular karyotyping in patients with SRS featuresJ Sachwitz, R Meyer, G Fekete, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failureF Haverkamp, J Wölfle, K Zerres, et al.
Clinical Nephrology|March 7, 2007
PDGF-B gene single-nucleotide polymorphisms are not predictive for disease onset or progression of IgA nephropathyB Bicanski, M Wenderdel, Peter R Mertens, et al.
Psychological Medicine|November 17, 2010
Effects of a CACNA1C genotype on attention networks in healthy individualsM Thimm, T Kircher, T Kellermann, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychiaC Bergmann, J Senderek, D Anhuf, et al.
Genomics|April 13, 1999
A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6J H Park, M P Dixit, L F Onuchic, et al.
Clinical Genetics|April 9, 2015
Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patientsS Rudnik-Schöneborn, D Tölle, J Senderek, et al.
Molecular Genetics and Metabolism|February 7, 2012
Life with too much polyprenol: polyprenol reductase deficiencyJ E H Gründahl, Z Guan, S Rust, et al.
Pageof 18

Showing results (161-170 of 174) with videos related to

Sort By:
Pageof 18
Neuroimage|June 6, 2009
Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individualsV Markov, A Krug, S Krach, et al.
Neurology|March 26, 2003
Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathyS Rudnik-Schöneborn, H H Goebel, W Schlote, et al.
Clinical Genetics|May 14, 2016
NSD1 duplication in Silver-Russell syndrome (SRS): molecular karyotyping in patients with SRS featuresJ Sachwitz, R Meyer, G Fekete, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failureF Haverkamp, J Wölfle, K Zerres, et al.
Clinical Nephrology|March 7, 2007
PDGF-B gene single-nucleotide polymorphisms are not predictive for disease onset or progression of IgA nephropathyB Bicanski, M Wenderdel, Peter R Mertens, et al.
Psychological Medicine|November 17, 2010
Effects of a CACNA1C genotype on attention networks in healthy individualsM Thimm, T Kircher, T Kellermann, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychiaC Bergmann, J Senderek, D Anhuf, et al.
Genomics|April 13, 1999
A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6J H Park, M P Dixit, L F Onuchic, et al.
Clinical Genetics|April 9, 2015
Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patientsS Rudnik-Schöneborn, D Tölle, J Senderek, et al.
Molecular Genetics and Metabolism|February 7, 2012
Life with too much polyprenol: polyprenol reductase deficiencyJ E H Gründahl, Z Guan, S Rust, et al.
Pageof 18