Mutational Analysis and Genotype-Phenotype Correlation in Patients with Classic 21-Hydroxylase Deficiency from Transylvania (North-West Romania)

Verfasser / Beitragende:
[A. Grigorescu-Sido,, E. Schulze,, P. Grigorescu-Sido,, U. Heinrich,, Τ. Nistor,, I. Duncea,]
Ort, Verlag, Jahr:
2002
Enthalten in:
Journal of Pediatric Endocrinology and Metabolism, 15/9(2002-11), 1505-1514
Format:
Artikel (online)
ID: 378737600