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Showing results (451-460 of 727) with videos related to

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American Journal of Human Genetics|May 7, 2002
PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneityMarco Tartaglia, Kamini Kalidas, Adam Shaw, et al.
Human Reproduction (Oxford, England)|September 25, 2021
Liquid biopsy: state of reproductive medicine and beyondGaby Schobers, Rebekka Koeck, Dominique Pellaers, et al.
Oncogene|August 29, 2012
GAB2 induces tumor angiogenesis in NRAS-driven melanomaY Yang, J Wu, A Demir, et al.
British Journal of Cancer|April 25, 2007
Patients with an unexplained microsatellite instable tumour have a low risk of familial cancerL I H Overbeek, C M Kets, K M Hebeda, et al.
Clinical Endocrinology|February 19, 2002
Leydig cell hypoplasia: cases with new mutations, new polymorphisms and cases without mutations in the luteinizing hormone receptor geneA Richter-Unruh, J W M Martens, M Verhoef-Post, et al.
Human Mutation|July 30, 2013
Detection of clinically relevant copy number variants with whole-exome sequencingJoep de Ligt, Philip M Boone, Rolph Pfundt, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 12, 2005
A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndromeE Kalay, A P M de Brouwer, R Caylan, et al.
JIMD Reports|March 17, 2021
Monoamine oxidase A activity in fibroblasts as a functional confirmation of <i>MAOA</i> variantsTessa M A Peters, Irma Lammerts van Bueren, Ben P B H Geurtz, et al.
American Journal of Human Genetics|February 11, 1999
Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27H van Bokhoven, M Jung, A P Smits, et al.
Journal of Medical Genetics|June 3, 2004
High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisationJ A Veltman, H G Yntema, D Lugtenberg, et al.
Pageof 73

Showing results (451-460 of 727) with videos related to

Sort By:
Pageof 73
American Journal of Human Genetics|May 7, 2002
PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneityMarco Tartaglia, Kamini Kalidas, Adam Shaw, et al.
Human Reproduction (Oxford, England)|September 25, 2021
Liquid biopsy: state of reproductive medicine and beyondGaby Schobers, Rebekka Koeck, Dominique Pellaers, et al.
Oncogene|August 29, 2012
GAB2 induces tumor angiogenesis in NRAS-driven melanomaY Yang, J Wu, A Demir, et al.
British Journal of Cancer|April 25, 2007
Patients with an unexplained microsatellite instable tumour have a low risk of familial cancerL I H Overbeek, C M Kets, K M Hebeda, et al.
Clinical Endocrinology|February 19, 2002
Leydig cell hypoplasia: cases with new mutations, new polymorphisms and cases without mutations in the luteinizing hormone receptor geneA Richter-Unruh, J W M Martens, M Verhoef-Post, et al.
Human Mutation|July 30, 2013
Detection of clinically relevant copy number variants with whole-exome sequencingJoep de Ligt, Philip M Boone, Rolph Pfundt, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 12, 2005
A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndromeE Kalay, A P M de Brouwer, R Caylan, et al.
JIMD Reports|March 17, 2021
Monoamine oxidase A activity in fibroblasts as a functional confirmation of <i>MAOA</i> variantsTessa M A Peters, Irma Lammerts van Bueren, Ben P B H Geurtz, et al.
American Journal of Human Genetics|February 11, 1999
Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27H van Bokhoven, M Jung, A P Smits, et al.
Journal of Medical Genetics|June 3, 2004
High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisationJ A Veltman, H G Yntema, D Lugtenberg, et al.
Pageof 73