Related Experiment Video

Updated: Jul 3, 2026

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
09:16

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants

Published on: February 21, 2015

Investigation of 4q-deletion in two unrelated patients using array CGH

S S Kaalund1, R S Møller, A Tészás

  • 1Department of Cellular and Molecular Medicine, Wilhelm Johannsen Centre for Functional Genome Research, University of Copenhagen, Copenhagen, Denmark.

American Journal of Medical Genetics. Part A
|August 9, 2008
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform
09:30

Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform

Published on: August 17, 2022

Technical Demonstration of Whole Genome Array Comparative Genomic Hybridization
16:37

Technical Demonstration of Whole Genome Array Comparative Genomic Hybridization

Published on: August 5, 2008

Related Experiment Videos

Last Updated: Jul 3, 2026

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
09:16

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants

Published on: February 21, 2015

Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform
09:30

Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform

Published on: August 17, 2022

Technical Demonstration of Whole Genome Array Comparative Genomic Hybridization
16:37

Technical Demonstration of Whole Genome Array Comparative Genomic Hybridization

Published on: August 5, 2008

Related Concept Videos

Karyotyping01:17

Karyotyping

Describing the number and physical features of chromosomes can reveal abnormalities that underlie genetic diseases. This description is facilitated by special staining techniques that produce a particular banding pattern on each chromosome. State-of-the-art techniques make this approach even more powerful, enabling the detection of individual genes that cause disease.A Simple Chromosome Staining Technique Provides Valuable Scientific InsightSome genetic diseases can be detected by looking at...

Articles linked to this work by shared authors, journal, and citation graph.

Oral hygiene management in critically ill patients: prevention of ventilator-associated pneumonia.

Frontiers in dental medicine·2026

Reference intervals for serum macro- and microminerals in clinically healthy horses in Northwestern Spain: Influence of age, sex, breed and diet.

Journal of equine veterinary science·2026

Use of SCORE2 in the assessment and control of cardiovascular risk in an apparently healthy individuals' cohort.

Revista clinica espanola·2025

EFFECTS OF MELANOPROTEINS AND THEIR PRECURSORS ON CELL PROLIFERATION THE PROBLEM OF SELECTIVITY.

Development, growth & differentiation·2023

Serotonin Type 2a Receptor in the Prefrontal Cortex Controls Perirhinal Cortex Excitability During Object Recognition Memory Recall.

Neuroscience·2022

The MAPKinase Signaling and the Stimulatory Protein-1 (Sp1) Transcription Factor Are Involved in the Phototherapy Effect on Cytokines Secretion from Human Bronchial Epithelial Cells Stimulated with Cigarette Smoke Extract.

Inflammation·2021

Exome Sequencing Uncovers Phenotypic and Genotypic Heterogeneity in 196 Indian Families Evaluated for Autoinflammatory Disorders.

American journal of medical genetics. Part A·2026

The Evaluation of Molecular Genetics and Clinical Manifestations in Patients With LZTR1-Associated Noonan Syndrome: A Retrospective Chart Review and Review of Literature.

American journal of medical genetics. Part A·2026

Expanding the Genotypic and Phenotypic Spectrum of Vissers-Bodmer Syndrome.

American journal of medical genetics. Part A·2026

Clinical and Functional Characterization of Gain-of-Function ABL1 Variants Expands the Phenotypic Spectrum of CHDSKM.

American journal of medical genetics. Part A·2026

Expanding the Clinical and Genetic Spectrum of Schmid Metaphyseal Chondrodysplasia: A Seven-Patient Series Including a Rare Homozygous COL10A1 Case.

American journal of medical genetics. Part A·2026

Rapid Genomic Testing: A Study of Institutional Utilization and Outcomes.

American journal of medical genetics. Part A·2026

Organelle partitioning in the multi-budding yeast Aureobasidium pullulans.

Molecular biology of the cell·2026

Pronuclear Transfer and Maternal Spindle Transfer in the Mouse.

Methods in molecular biology (Clifton, N.J.)·2026

Molecular architecture and spatial organization of proteasomes in the human sperm nucleus.

Nature structural & molecular biology·2026

Resolving missing human polymorphic inversions and other complex variants from ultra-long read data.

Genome research·2026

Mitochondrial Complex I at the Crossroads of NK cell Dysfunction in Glioblastoma.

Cancer discovery·2026

A Novel Sparse Cellular Labeling System with Tunable Gradients and Long-Term Stability.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026
See all related articles
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies
Jove
Visualize
Contact Us