Related Experiment Videos
Evidence for mutation being the source of the abnormal gene for plasma cholinesterase
Journal of Medical Genetics
|June 1, 1974
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Effects of dietary sulphur sources on concentrations of hydrogen sulphide in the rumen head-space gas of dairy cows.
Animal : an international journal of animal bioscience·2012
Enzymatic activity of albumin shown by coelenterazine chemiluminescence.
Luminescence : the journal of biological and chemical luminescence·2012
Comparison of red clover and ryegrass silage for dry cows and influence on subsequent lactation performance.
Journal of dairy science·2008
Effects of dairy cow diet forage proportion on duodenal nutrient supply and urinary purine derivative excretion.
Journal of dairy science·2006
Hypertrophic cardiomyopathy: a genome-wide association meta-analysis and polygenic risk score.
Journal of medical genetics·2026
Exome sequencing and large-scale analysis of electronic medical record-linked biobank data identify candidate deafness genes.
Journal of medical genetics·2026
Exploring the clinical and mutational spectrum of MORC2-associated disorders.
Journal of medical genetics·2026
Founder variant in OTOG causing non-syndromic sensorineural hearing loss in Irish traveller population.
Journal of medical genetics·2026
Risk of breast cancer after ovarian cancer in germline BRCA1/2 heterozygotes.
Journal of medical genetics·2026
Rapid minigene workflow for functional reclassification of splicing variants in hereditary cancer diagnostics.
Journal of medical genetics·2026
[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].
Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences·2026
Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.
Biology of sex differences·2026
Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.
Journal of assisted reproduction and genetics·2026
Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.
American journal of human genetics·2026