Related Experiment Videos
Indications for prenatal detection of genetic disorders
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32.
American journal of human genetics·2001
Chromosome 18q paracentric inversion in a family with mental retardation and hearing loss.
American journal of medical genetics·1998
CNS malformation in a child with Kabuki (Niikawa-Kuroki) syndrome: report and review.
American journal of medical genetics·1997
Terminal deletion of the long arm of chromosome 4 in a mother and two sons.
Clinical genetics·1996
Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes.
Journal of medical genetics·1995
Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21.
Cytogenetics and cell genetics·1995
High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.
The Journal of heredity·2026
Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.
Pediatrics international : official journal of the Japan Pediatric Society·2026
Proteome-wide QTL mapping enables gene-protein-phenotype metabolic network construction in a genetically diverse MASLD mouse model.
bioRxiv : the preprint server for biology·2026
Sequence determinants of pathogenicity in glucose-6-phosphatase linked to glycogen storage disease type 1a.
bioRxiv : the preprint server for biology·2026
Estimating the Penetrance of PRNP Mutations in Chinese Prion Disease Patients based on the Genome Databases.
Genomics, proteomics & bioinformatics·2026
Genome-wide linkage and association mapping identified a novel candidate gene, TaGLK-A1, underlying fructan content in wheat grain.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2026