Related Experiment Videos
Two additional RFLPs at the D4S10 locus, useful for Huntington's disease (HD)-family studies
E Bakker1, M I Skraastad, Y M Fisser-Groen
1Department of Human Genetics, Sylvius Laboratories, Leiden, The Netherlands.
Nucleic Acids Research
|November 11, 1987
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Bicontinuous Structure Mediated Microstructural Engineering of Hard Carbon for Enhanced Sodium Storage.
Advanced materials (Deerfield Beach, Fla.)·2025
[An International Urogynecological Association (IUGA)/International Continence Society (ICS) joint report on the terminology for the conservative and non-pharmacological management of female pelvic floor dysfunction].
Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie·2019
[Pelvic floor muscle training and pelvic floor disorders in women].
Gynecologie, obstetrique & fertilite·2015
[Evaluation of the electromyography activity of pelvic floor muscle during postural exercises using the Wii Fit Plus©. Analysis and perspectives in rehabilitation].
Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie·2014
A transcription factor regulatory atlas for activity inference and perturbation prediction.
Nucleic acids research·2026
Functional impact of Nth like DNA glycosylase 1 on mitochondrial dynamics.
Nucleic acids research·2026
UFold-X: an enhanced Dual & Dynamic U-Mamba model for long-range RNA secondary structure prediction.
Nucleic acids research·2026
Network analysis of the genetic relationships between twenty psychiatric and substance use disorders.
World psychiatry : official journal of the World Psychiatric Association (WPA)·2026
Clinical Utility of Trio Exome Sequencing in Rwandan Children With Autism Spectrum Disorder.
Molecular genetics & genomic medicine·2026
Large-Scale Neuroimaging and Genetic Analyses of the Human Thalamus in Loneliness.
Biological psychiatry global open science·2026
A recurrent CCDC82 frameshift variant associated with syndromic neurodevelopmental disorder in a consanguineous Pakistani family.
Biochemistry and biophysics reports·2026