Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidismEva Al Taji, Heiko Krude, Heike Biebermann et al.|European Journal of Endocrinology|2007Cited by 105
Guidelines for neonatal screening programmes for congenital hypothyroidismJ E Toublanc, M Klett, P Rochiccioli et al.|European Journal of Pediatrics|1993Cited by 43
Guidelines for Neonatal Screening Programs for Congenital HypothyroidismF Delange, G Giovannelli, M Klett et al.|Hormone Research|2008Cited by 14