Congenital anomalies associated with congenital hypothyroidism

Annales de Genetique

Volumn 42, Issue 1, 1999, Pages 17-20

  Stoll, C ^a   Dott, B ^a   Alembik, Y ^a   Koehl, C ^a  

^a UNIVERSITY HOSPITAL OF STRASBOURG   (France)

Author keywords

Congenital anomalies; Neonatal screening; Primary congenital hypothyroidism

Indexed keywords

ARTICLE; CONGENITAL HEART MALFORMATION; CONGENITAL HYPOTHYROIDISM; CONGENITAL MALFORMATION; DISEASE ASSOCIATION; HUMAN; MAJOR CLINICAL STUDY; NEWBORN; NEWBORN SCREENING;

ABNORMALITIES; CONGENITAL HYPOTHYROIDISM; FEMALE; FRANCE; HUMANS; HYPOTHYROIDISM; INCIDENCE; INFANT, NEWBORN; MALE; THYROTROPIN;

EID: 0033010634     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (16)