Answers are grounded in this paper and cite their sources.
A founder transgenic mouse harbored two different integration patterns of a transgene at the same locus, each of which gave rise to a similar autosomal recessive mutation. Mice of the mutant phenotype were of small stature but had normal levels of growth hormone. The disrupted locus was cloned, and a genetic and molecular analysis showed that the insertional mutants were allelic to a spontaneous mutant, pygmy. The mice should be a useful model for the growth hormone-resistant human dwarf syndromes and could lead to a greater understanding of the pathways involved in growth and development.
No takes yet. Share an insight, caveat, or question.
Xiang et al. (1990) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: