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Thomas Eggermann

Showing results (11-20 of 269) with videos related to

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Human Genetics|February 14, 2007
Gene symbol: SLC3A1. Disease: Cystinuria. Accession #Hm0547Eva Brauers, Thomas Eggermann
Human Genetics|February 14, 2007
Gene symbol: SLC3A1. Disease: Cystinuria. Accession #Hm0546Eva Brauers, Thomas Eggermann
Frontiers in Genetics|June 19, 2024
Molecular mechanisms of human overgrowth and use of <i>omics</i> in its diagnostics: chances and challengesDirk Prawitt, Thomas Eggermann
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|October 29, 2003
Uniparental disomy and Robertsonian translocations: risk estimation and prenatal testingThomas Eggermann, Klaus Zerres
Human Genetics|February 14, 2007
Gene symbol: SLC7A9. Disease: Cystinuria. Accession #Hm0545Eva Brauers, Thomas Eggermann
Expert Review of Endocrinology & Metabolism|November 15, 2022
Further understanding of paternal uniparental disomy in Beckwith-Wiedemann syndromeThomas Eggermann, Dirk Prawitt
Clinical Epigenetics|February 5, 2021
Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domainsThomas Eggermann, Matthias Begemann, Lutz Pfeiffer
Trends in Genetics : TIG|March 11, 2008
Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndromeThomas Eggermann, Katja Eggermann, Nadine Schönherr
Orphanet Journal of Rare Diseases|April 7, 2012
Cystinuria: an inborn cause of urolithiasisThomas Eggermann, Andreas Venghaus, Klaus Zerres
International Journal of Molecular Sciences|August 31, 2019
Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders: Characterization of Basic Mechanisms to Improve Clinical ManagementKatharina Wesseler, Florian Kraft, Thomas Eggermann
Pageof 27

Showing results (11-20 of 269) with videos related to

Sort By:
Pageof 27
Human Genetics|February 14, 2007
Gene symbol: SLC3A1. Disease: Cystinuria. Accession #Hm0547Eva Brauers, Thomas Eggermann
Human Genetics|February 14, 2007
Gene symbol: SLC3A1. Disease: Cystinuria. Accession #Hm0546Eva Brauers, Thomas Eggermann
Frontiers in Genetics|June 19, 2024
Molecular mechanisms of human overgrowth and use of <i>omics</i> in its diagnostics: chances and challengesDirk Prawitt, Thomas Eggermann
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|October 29, 2003
Uniparental disomy and Robertsonian translocations: risk estimation and prenatal testingThomas Eggermann, Klaus Zerres
Human Genetics|February 14, 2007
Gene symbol: SLC7A9. Disease: Cystinuria. Accession #Hm0545Eva Brauers, Thomas Eggermann
Expert Review of Endocrinology & Metabolism|November 15, 2022
Further understanding of paternal uniparental disomy in Beckwith-Wiedemann syndromeThomas Eggermann, Dirk Prawitt
Clinical Epigenetics|February 5, 2021
Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domainsThomas Eggermann, Matthias Begemann, Lutz Pfeiffer
Trends in Genetics : TIG|March 11, 2008
Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndromeThomas Eggermann, Katja Eggermann, Nadine Schönherr
Orphanet Journal of Rare Diseases|April 7, 2012
Cystinuria: an inborn cause of urolithiasisThomas Eggermann, Andreas Venghaus, Klaus Zerres
International Journal of Molecular Sciences|August 31, 2019
Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders: Characterization of Basic Mechanisms to Improve Clinical ManagementKatharina Wesseler, Florian Kraft, Thomas Eggermann
Pageof 27