Congenital hypothyroidism detected by neonatal screening: relationship between biochemical severity and early clinical features.

Author:

Grant D B,Smith I,Fuggle P W,Tokar S,Chapple J

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference20 articles.

1. Social Security. Screening for early detection of congenital hypothyroidism;Department of Health and,1981

2. Survey of neonatal screening for primary hypothyroidism;Grant, D.B.; Smith, I.;England, Wales and Northern Ireland; BMJ,1982

3. Population screening for congenital hypothyroidism;Hulse, J.A.; Grant, D.B.; Clayton, B.E.;BMJ,1980

4. Screening for congenital hypothyroidism with specimen collection at two time periods: results of the Northwest Region Screening Program;LaFranchi, S.H.; Hanna, C.E.; Krinnz, P.L.; Skeels, M.R.; Miyahira, R.S.; Sesser, D.E.;Pediatrics,1985

5. Le depistage neonatal de l'hypothyroidie en France;Rochiccioli, P.; Dutau, G.; Roge, B.; Petrus, M.; Augier, D.; Enjaume, C.;J Genet Hum,1981

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