A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: Data from the Italian registry for congenital hypothyroidism (1991-1998)

Journal of Clinical Endocrinology and Metabolism

Volumn 87, Issue 2, 2002, Pages 557-562

  Olivieri, A ^a   Stazi, M A ^a   Mastroiacovo, P ^b   Fazzini, C ^c   Medda, E ^b   Spagnolo, A ^a   De Angelis, S ^b   Grandolfo, M E ^b   Taruscio, D ^a   Cordeddu, V ^a   Sorcini, M ^b  

^a ISTITUTO SUPERIORE DI SANITÀ   (Italy)

^b CATHOLIC UNIVERSITY   (Italy)

^c Italian Institute of Social Medicine   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CONGENITAL HYPOTHYROIDISM; CONGENITAL MALFORMATION; DATA ANALYSIS; EARLY DIAGNOSIS; EMBRYO DEVELOPMENT; FEMALE; FOLLOW UP; GENE FREQUENCY; HUMAN; INFANT; ITALY; MAJOR CLINICAL STUDY; MALE; NEWBORN SCREENING; POPULATION RESEARCH; PREVALENCE; PRIORITY JOURNAL; THYROID FOLLICLE CELL;

ABNORMALITIES; ABNORMALITIES, MULTIPLE; CONGENITAL HYPOTHYROIDISM; EYE ABNORMALITIES; FEMALE; HUMANS; HYPOTHYROIDISM; INCIDENCE; INFANT; INFANT, NEWBORN; ITALY; MALE; NEONATAL SCREENING; NERVOUS SYSTEM MALFORMATIONS; PREVALENCE; REGISTRIES;

EID: 18244368524     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.87.2.557     Document Type: Article

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