Newborn screening for congenital hypothyroidism, Victoria, Australia, 1977-1997. Part 1: The screening programme, demography, baseline perinatal data and diagnostic classification

Journal of Pediatric Endocrinology and Metabolism

Volumn 14, Issue 9, 2001, Pages 1597-1610

  Connelly, J F ^a   Coakley, J C ^a   Gold, H ^a   Francis, I ^a   Mathur, K S ^a   Rickards, A L ^a   Price, G J ^a   Halliday, J L ^a   Wolfe, R ^a  

^a NONE   (Australia)

Author keywords

Baseline; Classification; Congenital hypothyroidism; Demography; Newborn screening; Victoria

Indexed keywords

PERTECHNETIC ACID TC 99M; THYROXINE;

APLASIA; ARTICLE; AUSTRALIA; CLINICAL FEATURE; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; DEMOGRAPHY; DISEASE CLASSIFICATION; DISEASE PREDISPOSITION; DYSPLASIA; ECTOPIC THYROID GLAND; ETHNOLOGY; FEMALE; HUMAN; INFANT; LABOR INDUCTION; LABORATORY DIAGNOSIS; LONGITUDINAL STUDY; MAJOR CLINICAL STUDY; MALE; MIDDLE EAST; NEUROPSYCHOLOGY; NEWBORN; NEWBORN SCREENING; PARENT; PATHOGENESIS; PERINATAL PERIOD; PROSPECTIVE STUDY; SEX DIFFERENCE; THYROXINE BLOOD LEVEL;

EID: 0035673475     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: 10.1515/JPEM.2001.14.9.1597     Document Type: Article

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