https://pubmed.ncbi.nlm.nih.gov/32112393/
A GLI3 variant leading to polydactyly in heterozygotes and Pallister-Hall-like syndrome in a...
Variants in transcriptional activator Gli Kruppel Family Member 3 (GLI3) have been reported to be associated with several phenotypes including Greig...
https://pmc.ncbi.nlm.nih.gov/articles/PMC21137/
Knockout of the abetalipoproteinemia gene in mice: Reduced lipoprotein secretion in heterozygotes...
Abetalipoproteinemia, an inherited human disease characterized by a near-complete absence of the apolipoprotein (apo) B-containing lipoproteins in the plasma,...
of theknockoutabetalipoproteinemiagene
https://www.wikidata.org/wiki/Q33710897
The distribution of x-ray induced crossovers from Curly inversion heterozygotes of drosophila...
scientific article published on 01 October 1950
x ray