Neonatal thyroid disorders

Hormone Research

Volumn 59, Issue SUPPL. 1, 2003, Pages 24-29

  Grüters, Annette ^a   Biebermann, Heike ^a   Krude, Heiko ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

Author keywords

Disorders; Neonatal; Thyroid

Indexed keywords

PENDRIN; PROTIRELIN; PROTIRELIN RECEPTOR; SODIUM IODIDE SYMPORTER; THYROID PEROXIDASE; THYROTROPIN; THYROTROPIN RECEPTOR; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR LHX3; TRANSCRIPTION FACTOR NKX2 1; TRANSCRIPTION FACTOR PAX8; TRANSCRIPTION FACTOR TTF 2; UNCLASSIFIED DRUG;

AUTOSOMAL RECESSIVE INHERITANCE; CENTRAL NERVOUS SYSTEM; CHILD DEVELOPMENT; CONFERENCE PAPER; CONGENITAL HYPOTHYROIDISM; DEVELOPMENTAL DISORDER; DIAGNOSTIC PROCEDURE; DOMINANT INHERITANCE; EARLY DIAGNOSIS; EMBRYO DEVELOPMENT; GENE FUNCTION; GENE IDENTIFICATION; GENE MUTATION; GENETIC CODE; HUMAN; HYPOPHYSIS; HYPOTHALAMUS; HYPOTHYROIDISM; MENTAL DEFICIENCY; MENTAL DEVELOPMENT; NERVOUS SYSTEM DEVELOPMENT; NEUROLOGIC DISEASE; NEWBORN; NEWBORN DISEASE; NONHUMAN; PATIENT CARE; PATIENT COUNSELING; PEDIATRICS; PREVALENCE; PRIORITY JOURNAL; PROTEIN DEFECT; PROTEIN EXPRESSION; RECESSIVE INHERITANCE; SCREENING; THYROID DISEASE; THYROID GLAND; TREATMENT PLANNING;

ANIMALS; CONGENITAL HYPOTHYROIDISM; HUMANS; HYPOTHYROIDISM; INFANT, NEWBORN; IODIDE PEROXIDASE; MUTATION; NEONATAL SCREENING; RECEPTORS, THYROTROPIN; THYROID GLAND; TRANSCRIPTION FACTORS;

EID: 0037265467     PISSN: 03010163     EISSN: None     Source Type: Journal    
DOI: 10.1159/000067841     Document Type: Conference Paper

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