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1375066
1375066
https://w3id.org/oc/corpus/br/1375066
Bovine exome sequence analysis and targeted SNP genotyping of recessive fertility defects BH1, HH2, and HH3 reveal a putative causative mutation in SMC2 for HH3
P3181
3b1dafd2da9f2697a8cb51a0ddc04a4e96ce8c8a
P3181
Q27313562-4DA4B981-5658-47A7-A83C-2B5D1290607E
P3181
1375066
https://w3id.org/oc/corpus/br/1375066