Related Experiment Video

Updated: Apr 14, 2026

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

9.2K

Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary

Mindy H Li1,2, Kelly Arndt3, Soma Das3

  • 1Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

American Journal of Medical Genetics. Part A
|April 23, 2015
PubMed
Abstract

No abstract available in PubMed .

Keywords:
CDK5RAP2autosomal recessive primary microcephaly (MCPH)developmental delayfailure to thrivemicrocephalyspeech delay

More Related Videos

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model
05:12

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model

Published on: September 4, 2017

11.4K
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
06:41

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

Published on: August 20, 2019

14.5K

Related Experiment Videos

Last Updated: Apr 14, 2026

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

9.2K
Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model
05:12

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model

Published on: September 4, 2017

11.4K
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
06:41

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

Published on: August 20, 2019

14.5K

Related Concept Videos

Genetic Lingo01:11

Genetic Lingo

118.6K
Overview
118.6K
Incomplete Dominance01:43

Incomplete Dominance

32.8K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
32.8K
The Retinoblastoma Gene01:20

The Retinoblastoma Gene

5.0K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
5.0K
Pedigree Analysis01:35

Pedigree Analysis

91.4K
Overview
91.4K

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

AI at the Bedside: An Argument for a Training Wheels Approach.

Pediatrics·2026

Validity Evidence for the Better Research Interactions for Every Family (BRIEF) Assessment Tool.

Cureus·2026

Climate Stewardship in the Clinical Setting.

Advances in pediatrics·2026

Evaluation of the MAking DEcisions for Kids (MADE for Kids) Survey in a Simulated Setting.

Academic pediatrics·2026

A role for EHMT2 in a novel autosomal recessive neurodevelopmental syndrome? A case report.

Frontiers in genetics·2026

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study.

medRxiv : the preprint server for health sciences·2026

Novel Compound Heterozygous ATAD3A Variants in Harel-Yoon Syndrome With Congenital Cataracts and Dilated Cardiomyopathy.

American journal of medical genetics. Part A·2026

The Value of Integrating Adult Genetic Services Into Pregnancy Care: Changing Fetal, Neonatal, and Maternal Management.

American journal of medical genetics. Part A·2026

Systematic Review of Females With Intellectual Disability and MECP2 Duplication.

American journal of medical genetics. Part A·2026

TTC21B: From Modifier to Causative Gene in Joubert Syndrome.

American journal of medical genetics. Part A·2026

Fracture Prevalence Among Those With Hypermobility Spectrum Disorder/Hypermobile Ehlers-Danlos Syndrome.

American journal of medical genetics. Part A·2026

Height, Head Circumference, Sitting Height, Leg Length, and Body Proportions Growth References to the Argentinian and Spanish Population for Hypochondroplasia.

American journal of medical genetics. Part A·2026

Mortality Outcomes Following Pediatric Emergency Department Visits: A Systematic Review and Meta-Analysis.

Medical journal of the Islamic Republic of Iran·2026

Impact of respiratory support on time to achieve full oral feeding in very low birth weight infants: a retrospective study.

Frontiers in pediatrics·2026

Jujube pit ingestion leading to ileal perforation and secondary acute appendicitis in a child: a case report.

AME case reports·2026

Brain-computer interfaces in pediatric populations: research advances, application challenges, and future directions.

Frontiers in pediatrics·2026

Sleep Disturbances in Children and Adolescents with Autism Spectrum Disorder: A Scoping Review of Clinical Features, Impact and Interventions.

Indian journal of psychological medicine·2026

Immune system ontogeny-a subtle evolution to perfection.

Frontiers in aging·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