advertisement
Harto M-A 1
Showing records 1 to 1 | Display all abstracts from Harto M-A25263 Primary congenital glaucoma caused by the homozygous F261L CYP1B1 mutation and paternal isodisomy of chromosome 2
Lopez-Garrido M -P; Campos-Mollo E; Harto M-A; Escribano J
Clinical Genetics 2009; 76: 552-557
