Jove
Visualize
Contact Us
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

Related Experiment Videos

Tetranucleotide repeat polymorphism at the D11S488 locus

D Browne1, M Gen, G A Evans

  • 1Oregon Health Sciences University, Portland 97201.

Human Molecular Genetics
|January 1, 1993
PubMed
Summary

No abstract available in PubMed .

Related Experiment Videos

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Observation of disorder-free localization using a (2+1)D lattice gauge theory on a quantum processor.

Science (New York, N.Y.)·2026
Same author

Quintuplet Condensation in the Skyrmionic Insulator Cu_{2}OSeO_{3} at Ultrahigh Magnetic Fields.

Physical review letters·2026
Same author

Predictors of early ICU re-admission.

Irish medical journal·2024
Same author

Dimensional reduction and incommensurate dynamic correlations in the <math> </math> triangular-lattice antiferromagnet Ca<sub>3</sub>ReO<sub>5</sub>Cl<sub>2</sub>.

Nature communications·2022
Same author

Radiological investigations in non-aneurysmal subarachnoid haemorrhage: A 5-year review.

Brain & spine·2022
Same author

Case of Traumatic Tetanus-Recovery: Read before Medical Society, County Kings, N. Y.

The Southern medical record·2022
Same journal

Utrophin requires α-Syntrophin to maintain neuromuscular junction integrity in mdx mice.

Human molecular genetics·2026
Same journal

A novel gene ACTRT3 mutations induce sperm malformations and fertilization failure via Acrosomal ultrastructural defects.

Human molecular genetics·2026
Same journal

Nucleic acid-based therapeutic strategies for modulator-refractory cystic fibrosis-causing variants.

Human molecular genetics·2026
Same journal

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.

Human molecular genetics·2026
Same journal

Nicotinamide riboside prevents mitochondrial dysfunction in nemaline myopathy type 6.

Human molecular genetics·2026
Same journal

Retraction: Aqua-soluble DDQ reduces the levels of Dr1 and Ab and inhibits abnormal interactions between Ab and Dr1 and protects Alzheimer's disease neurons from Ab- and Dr1-induced mitochondrial and synaptic toxicities.

Human molecular genetics·2026
See all related articles