about
Compound heterozygous and homozygous mutations of the TSHbeta gene as a cause of congenital central hypothyroidism in Europe.Polycystic ovary syndrome: challenges in adolescence.Mutational characterization of steroid 21-hydroxylase gene in Portuguese patients with congenital adrenal hyperplasia.[Type 1b pseudohyperparathyroidism: a rare cause of syncope]Neonatal presentation of growth hormone deficiency in CHARGE syndrome: the benefit of early treatment on long-term growth
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Manuel Fontoura
@ast
Manuel Fontoura
@en
Manuel Fontoura
@es
Manuel Fontoura
@nl
Manuel Fontoura
@pt
Manuel Fontoura
@sl
type
label
Manuel Fontoura
@ast
Manuel Fontoura
@en
Manuel Fontoura
@es
Manuel Fontoura
@nl
Manuel Fontoura
@pt
Manuel Fontoura
@sl
prefLabel
Manuel Fontoura
@ast
Manuel Fontoura
@en
Manuel Fontoura
@es
Manuel Fontoura
@nl
Manuel Fontoura
@pt
Manuel Fontoura
@sl
P106
P1153
6701825399
P21
P31
P496
0000-0001-6990-4583