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Peter Bauer

Showing results (411-420 of 585) with videos related to

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Frontiers in Genetics|August 21, 2019
Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive FamiliesLior Greenbaum, Ben Pode-Shakked, Shlomit Eisenberg-Barzilai, et al.
International Journal of Molecular Sciences|October 23, 2019
Determination of the Pathological Features of NPC1 Variants in a Cellular Complementation TestXiao Feng, Claudia Cozma, Supansa Pantoom, et al.
The Journal of Allergy and Clinical Immunology|January 28, 2014
Early-life determinants of asthma from birth to age 20 years: a German birth cohort studyLinus B Grabenhenrich, Hannah Gough, Andreas Reich, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|May 27, 2015
Allergic multimorbidity of asthma, rhinitis and eczema over 20 years in the German birth cohort MASHannah Gough, Linus Grabenhenrich, Andreas Reich, et al.
Journal of Medical Genetics|August 31, 2016
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrumMiriam S Reuter, Angelika Riess, Ute Moog, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 30, 2026
Lack of Cerebrospinal Fluid α-Synuclein Seeding in VPS35 D620N- and LRRK2 Y1699C-Linked Parkinson's DiseaseLetizia Santinelli, Neringa Pratuseviciute, Lara M Lange, et al.
Clinical Nutrition (Edinburgh, Scotland)|May 16, 2006
The German hospital malnutrition studyMatthias Pirlich, Tatjana Schütz, Kristina Norman, et al.
NPJ Genomic Medicine|October 21, 2020
Genomic testing in 1019 individuals from 349 Pakistani families results in high diagnostic yield and clinical utilityHuma Cheema, Aida M Bertoli-Avella, Volha Skrahina, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 26, 2024
Genetic and Epidemiological Insights into RAB32-Linked Parkinson's DiseaseMandy Radefeldt, Sabrina Lemke, Kridsadakorn Chaichoompu, et al.
Human Mutation|September 15, 2004
Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7)Robert Hering, Karsten M Strauss, Xiao Tao, et al.
Pageof 59

Showing results (411-420 of 585) with videos related to

Sort By:
Pageof 59
Frontiers in Genetics|August 21, 2019
Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive FamiliesLior Greenbaum, Ben Pode-Shakked, Shlomit Eisenberg-Barzilai, et al.
International Journal of Molecular Sciences|October 23, 2019
Determination of the Pathological Features of NPC1 Variants in a Cellular Complementation TestXiao Feng, Claudia Cozma, Supansa Pantoom, et al.
The Journal of Allergy and Clinical Immunology|January 28, 2014
Early-life determinants of asthma from birth to age 20 years: a German birth cohort studyLinus B Grabenhenrich, Hannah Gough, Andreas Reich, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|May 27, 2015
Allergic multimorbidity of asthma, rhinitis and eczema over 20 years in the German birth cohort MASHannah Gough, Linus Grabenhenrich, Andreas Reich, et al.
Journal of Medical Genetics|August 31, 2016
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrumMiriam S Reuter, Angelika Riess, Ute Moog, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 30, 2026
Lack of Cerebrospinal Fluid α-Synuclein Seeding in VPS35 D620N- and LRRK2 Y1699C-Linked Parkinson's DiseaseLetizia Santinelli, Neringa Pratuseviciute, Lara M Lange, et al.
Clinical Nutrition (Edinburgh, Scotland)|May 16, 2006
The German hospital malnutrition studyMatthias Pirlich, Tatjana Schütz, Kristina Norman, et al.
NPJ Genomic Medicine|October 21, 2020
Genomic testing in 1019 individuals from 349 Pakistani families results in high diagnostic yield and clinical utilityHuma Cheema, Aida M Bertoli-Avella, Volha Skrahina, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 26, 2024
Genetic and Epidemiological Insights into RAB32-Linked Parkinson's DiseaseMandy Radefeldt, Sabrina Lemke, Kridsadakorn Chaichoompu, et al.
Human Mutation|September 15, 2004
Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7)Robert Hering, Karsten M Strauss, Xiao Tao, et al.
Pageof 59