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Martin Poot

Showing results (41-50 of 100) with videos related to

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Molecular Syndromology|March 30, 2016
From Telomere Crisis via Dicentric Chromosomes to Kataegis and ChromothripsisMartin Poot
Molecular Syndromology|December 13, 2017
Neocentromeres to the Rescue of Acentric Chromosome FragmentsMartin Poot
Molecular Syndromology|July 8, 2016
The Growing Complexity of the Monosomy 1p36 SyndromeMartin Poot
Molecular Syndromology|November 23, 2020
Fanconi Anemia: A Syndrome of Anemia and Skeletal Malformations Progressing to a Gene Network Involved in Genomic Stability and Malignant DiseaseMartin Poot
Molecular Syndromology|January 2, 2023
Expanded Phenotypic Spectrum or Multiple Syndromes?Martin Poot
Molecular Syndromology|April 13, 2019
Structural Genome Variations Related to CraniosynostosisMartin Poot
Molecular Syndromology|June 14, 2019
Phenotypic Spectrum and Severity of Disease Depending on the Mutated Protein Domain of NMDA Receptor-Encoding GenesMartin Poot
Molecular Syndromology|January 7, 2016
Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome RearrangementsMartin Poot, Thomas Haaf
Molecular Syndromology|March 29, 2021
Prevalence and Phenotypic Impact of Robertsonian TranslocationsMartin Poot, Ron Hochstenbach
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2010
A three-step workflow procedure for the interpretation of array-based comparative genome hybridization results in patients with idiopathic mental retardation and congenital anomaliesMartin Poot, Ron Hochstenbach
Pageof 10

Showing results (41-50 of 100) with videos related to

Sort By:
Pageof 10
Molecular Syndromology|March 30, 2016
From Telomere Crisis via Dicentric Chromosomes to Kataegis and ChromothripsisMartin Poot
Molecular Syndromology|December 13, 2017
Neocentromeres to the Rescue of Acentric Chromosome FragmentsMartin Poot
Molecular Syndromology|July 8, 2016
The Growing Complexity of the Monosomy 1p36 SyndromeMartin Poot
Molecular Syndromology|November 23, 2020
Fanconi Anemia: A Syndrome of Anemia and Skeletal Malformations Progressing to a Gene Network Involved in Genomic Stability and Malignant DiseaseMartin Poot
Molecular Syndromology|January 2, 2023
Expanded Phenotypic Spectrum or Multiple Syndromes?Martin Poot
Molecular Syndromology|April 13, 2019
Structural Genome Variations Related to CraniosynostosisMartin Poot
Molecular Syndromology|June 14, 2019
Phenotypic Spectrum and Severity of Disease Depending on the Mutated Protein Domain of NMDA Receptor-Encoding GenesMartin Poot
Molecular Syndromology|January 7, 2016
Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome RearrangementsMartin Poot, Thomas Haaf
Molecular Syndromology|March 29, 2021
Prevalence and Phenotypic Impact of Robertsonian TranslocationsMartin Poot, Ron Hochstenbach
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2010
A three-step workflow procedure for the interpretation of array-based comparative genome hybridization results in patients with idiopathic mental retardation and congenital anomaliesMartin Poot, Ron Hochstenbach
Pageof 10