Related Experiment Video

Updated: Sep 20, 2025

Transuterine Fetal Tracheal Occlusion Model in Mice
06:31

Transuterine Fetal Tracheal Occlusion Model in Mice

Published on: February 5, 2021

3.2K

Evidence-Based Genetic Testing for Individuals with Congenital Diaphragmatic Hernia

Yoel Gofin1, Daryl A Scott2

  • 1Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas; Texas Children's Hospital, Houston, Texas.

The Journal of Pediatrics
|June 6, 2022
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

Fetal Mouse Cardiovascular Imaging Using a High-frequency Ultrasound 30/45MHZ System
07:34

Fetal Mouse Cardiovascular Imaging Using a High-frequency Ultrasound 30/45MHZ System

Published on: May 5, 2018

11.8K
FISH for Pre-implantation Genetic Diagnosis
07:34

FISH for Pre-implantation Genetic Diagnosis

Published on: February 23, 2011

37.0K

Related Experiment Videos

Last Updated: Sep 20, 2025

Transuterine Fetal Tracheal Occlusion Model in Mice
06:31

Transuterine Fetal Tracheal Occlusion Model in Mice

Published on: February 5, 2021

3.2K
Fetal Mouse Cardiovascular Imaging Using a High-frequency Ultrasound 30/45MHZ System
07:34

Fetal Mouse Cardiovascular Imaging Using a High-frequency Ultrasound 30/45MHZ System

Published on: May 5, 2018

11.8K
FISH for Pre-implantation Genetic Diagnosis
07:34

FISH for Pre-implantation Genetic Diagnosis

Published on: February 23, 2011

37.0K

Related Concept Videos

Animal Mitochondrial Genetics02:59

Animal Mitochondrial Genetics

8.1K
Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
8.1K
Pedigree Analysis01:35

Pedigree Analysis

85.5K
Overview
85.5K

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

SPEN deficiency contributes to the development of orofacial clefts in humans and mice.

Human molecular genetics·2026

Neurodevelopmental Phenotypes and Brain Anomalies in Individuals With Heterozygous SEMA6A Variants.

Clinical genetics·2026

MAJIQ-CLIN: A novel tool to help identify Mendelian disease-causing variants from RNA-seq data.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

New genotype-phenotype correlations and management recommendations for individuals with RERE variants.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes.

Clinical genetics·2026

CUL3-Related Neurodevelopmental Disorder: Expanding the Prenatal Phenotype.

Prenatal diagnosis·2026

Infection Triggered Encephalopathies in Australian Children: A National Multicentre Case Series 2013-2024.

The Journal of pediatrics·2026

The Evolving Legal Landscape of Necrotizing Enterocolitis in Neonatology: What Years of Litigation Inform us About the Future.

The Journal of pediatrics·2026

Trends in Emergency Department Visits for Children, 2016-2023.

The Journal of pediatrics·2026

Multisystem Inflammatory Syndrome Therapies in Children: A Comparative Effectiveness Trial.

The Journal of pediatrics·2026

Postnatal Growth Patterns in Children Born at Term and Preterm in a Large Primary Care Network.

The Journal of pediatrics·2026

More Screens for Teens? The Incremental Value of Screening for Depression, Suicidality, and Anxiety in Pediatric Primary Care.

The Journal of pediatrics·2026

Genetic and stochastic basis of phenotypic discordance in 16p11.2 mouse model deletion.

bioRxiv : the preprint server for biology·2026

Genetics in Heterotaxy: A Case Series and Literature Review on DNAH9, PKD1L1, MMP21, and GDF1.

Clinical genetics·2026

DNA Methylation Profiling in IDH-Mutant Gliomas: Biological Evolution, Molecular Grading and Clinical Implementation.

Neuropathology and applied neurobiology·2026

Multiomic Single-Nucleus Profiling Reveals Cell-Type-Specific Epigenetic and Transcriptional Dysregulation in Major Depressive Disorder Brain.

The international journal of neuropsychopharmacology·2026

Serum Isthmin-1 in Gestational Diabetes Mellitus: A Case-Control Study Providing Preliminary Evidence of Elevated Levels and Association With Insulin Resistance.

Medical science monitor : international medical journal of experimental and clinical research·2026

Genomic structural equation modeling reveals novel genetic loci and pathways in panvascular disease.

Medicine·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