Rapid and Efficient Method for Detection of A/C 655G Mutation in Patients with Congenital Steroid 21-hydroxylase Deficiency | Charles Explorer

Rapid and Efficient Method for Detection of A/C 655G Mutation in Patients with Congenital Steroid 21-hydroxylase Deficiency

Publikace na Ústřední knihovna, 2. lékařská fakulta |

1996

Osoby