TY  - GEN
AU  - Ramos,Helton E
AU  - Labedan,Isabelle
AU  - Carré,Aurore
AU  - Castanet,Mireille
AU  - Guemas,Isabelle
AU  - Tron,Elodie
AU  - Madhi,Fouad
AU  - Delacourt,Christophe
AU  - Maciel,Rui M B
AU  - Polak,Michel
TI  - New cases of isolated congenital central hypothyroidism due to homozygous thyrotropin beta gene mutations: a pitfall to neonatal screening
SN  - 1557-9077
PY  - 2010///0920
KW  - Congenital Hypothyroidism
KW  - genetics
KW  - Consanguinity
KW  - Diagnostic Errors
KW  - Female
KW  - Homozygote
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Neonatal Screening
KW  - Pedigree
KW  - Thyrotropin
KW  - analysis
KW  - Thyrotropin, beta Subunit
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1089/thy.2009.0462
ER  -