Related Experiment Video

Updated: Nov 29, 2025

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

8.9K

Whole exome sequencing for developmental delay and learning difficulties: abridged secondary publication

S L J Kwok1, W L E Hau2, T F Chan3,4

  • 1School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong.

Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|November 24, 2020
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
05:51

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

Published on: June 15, 2011

26.2K
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
09:34

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

34.4K

Related Experiment Videos

Last Updated: Nov 29, 2025

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

8.9K
A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
05:51

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

Published on: June 15, 2011

26.2K
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
09:34

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

34.4K

Related Concept Videos

Next-generation Sequencing03:00

Next-generation Sequencing

96.3K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
96.3K
Learning Disabilities01:25

Learning Disabilities

447
Learning disabilities are cognitive disorders caused by neurological impairments that affect cognitive functions like language and reading, without indicating overall intellectual or developmental challenges. These disabilities differ from global intellectual or developmental disabilities as they are limited to distinct cognitive functions. Common learning disabilities include dysgraphia, dyslexia, and dyscalculia, each of which impacts unique aspects of learning.
Dyslexia
Dyslexia is a...
447
Sex-linked Disorders01:43

Sex-linked Disorders

106.1K
Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
106.1K

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

Urban green waste bulking agent is the major source of antimicrobial resistance genes persisted in home compost, not animal manure.

Environmental research·2023

What do psychiatrists think about primary mental health competencies among family doctors? A WPA-WONCA global survey.

BJPsych international·2021

Changes of the intestinal microbiota along the gut of Japanese Eel (Anguilla japonica).

Letters in applied microbiology·2021

Ancestral whole-genome duplication in the marine chelicerate horseshoe crabs.

Heredity·2017

Oncogenic mutations and dysregulated pathways in obesity-associated hepatocellular carcinoma.

Oncogene·2016

Ancestral whole-genome duplication in the marine chelicerate horseshoe crabs.

Heredity·2015

Embedding e-learning in postgraduate medical education: system-level barriers and enablers in Hong Kong.

Hong Kong medical journal = Xianggang yi xue za zhi·2026

A predictive model of survival in early-stage medullary breast carcinoma: a population-based study.

Hong Kong medical journal = Xianggang yi xue za zhi·2026

One-stop virtual planning for optimising implant selection and surgical efficiency in subtrochanteric fractures.

Hong Kong medical journal = Xianggang yi xue za zhi·2026

Trends and outcomes of massive primary postpartum haemorrhage and second-line therapy use: a retrospective study in a Hong Kong public hospital using the Hospital Authority electronic audit form.

Hong Kong medical journal = Xianggang yi xue za zhi·2026

Mid-term risk factor analysis and predictors of restenosis in patients undergoing carotid artery stenting.

Hong Kong medical journal = Xianggang yi xue za zhi·2026

Kidney health for all: caring for people, protecting the planet.

Hong Kong medical journal = Xianggang yi xue za zhi·2026

Haplotype-resolved genome assembly of a male Dioscorea alata cultivar reveals the structure and evolution of young sex chromosomes.

The Plant journal : for cell and molecular biology·2026

Low-Level Viremia and Spatial Heterogeneity Among Individuals on Dolutegravir-Based Antiretroviral Therapy in Botswana: A Nationwide Study (2016-2022).

The Journal of infectious diseases·2026

Migraine Headaches in a Pediatric Patient With SETD5-Related Neurodevelopmental Disorder and Inflammatory Comorbidities: A Case Report.

Cureus·2026

Spatial biases in visual feature representation of mouse dorsal lateral geniculate nucleus boutons.

iScience·2026

Dentate gyrus immaturity and region-specific synaptic and autophagy alterations across hippocampal subfields in schizophrenia.

Schizophrenia research·2026

A Novel de Novo WAC Frameshift Variant in DeSanto-Shinawi Syndrome With Temporo-Occipital Epileptiform Activity and Congenital Cardiac Anomalies.

American journal of medical genetics. Part A·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