Nineteen years of national screening for congenital hypothyroidism: Familial cases with thyroid dysgenesis suggest the involvement of genetic factors

Journal of Clinical Endocrinology and Metabolism

Volumn 86, Issue 5, 2001, Pages 2009-2014

  Castanet, Mireille ^a   Polak, Michel ^a   Bonaïti Pellié, Catherine ^c   Lyonnet, Stanislas ^b   Czernichow, Paul ^a   Léger, Juliane ^a  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c INSTITUT GUSTAVE ROUSSY   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL FEATURE; CONGENITAL HYPOTHYROIDISM; CONGENITAL MALFORMATION; ECTOPIC THYROID GLAND; FAMILIAL DISEASE; FEMALE; HEREDITY; HUMAN; MAJOR CLINICAL STUDY; MALE; NEWBORN; NEWBORN SCREENING; ORGANOGENESIS; PRIORITY JOURNAL; THYROID DISEASE;

EID: 0034999523     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jcem.86.5.7501     Document Type: Article

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