R. Pfaffle
AuthID: R-00G-9G8
1
TITLE: Compound heterozygous and homozygous mutations of the TSH beta gene as a cause of congenital central hypothyroidism in Europe
AUTHORS: Karges, B; LeHeup, B; Schoenle, E; Castro Correia, C; Fontoura, M ; Pfaffle, R; Andler, W; Debatin, KM; Karges, W;
PUBLISHED: 2004, SOURCE: HORMONE RESEARCH, VOLUME: 62, ISSUE: 3
AUTHORS: Karges, B; LeHeup, B; Schoenle, E; Castro Correia, C; Fontoura, M ; Pfaffle, R; Andler, W; Debatin, KM; Karges, W;
PUBLISHED: 2004, SOURCE: HORMONE RESEARCH, VOLUME: 62, ISSUE: 3
