Thyroid hemiagenesis is a rare variant of thyroid dysgenesis with a familial component but without Pax8 mutations in a cohort of 22 cases

Pediatric Research

Volumn 57, Issue 6, 2005, Pages 908-913

  Castanet, Mireille ^a   Leenhardt, Laurence ^b   Léger, Juliane ^a   Simon Carré, Aurore ^c   Lyonnet, Stanislas ^c   Pelet, Anna ^c   Czernichow, Paul ^a   Polak, Michel ^a,c  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR PAX8;

ADOLESCENT; ADULT; AGED; AGENESIS; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; COHORT ANALYSIS; FAMILIAL DISEASE; FAMILY HISTORY; FEMALE; GENE MUTATION; HEREDITY; HETEROZYGOSITY; HUMAN; MALE; ORGANOGENESIS; PATHOPHYSIOLOGY; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM; THYROGLOSSAL DUCT CYST; THYROID DISEASE; THYROID DYSGENESIS; THYROID HEMIAGENESIS;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; DNA; DNA-BINDING PROTEINS; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; NUCLEAR PROTEINS; PAIRED BOX TRANSCRIPTION FACTORS; PEDIGREE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; THYROID GLAND; TRANS-ACTIVATORS;

EID: 19444374566     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/01.PDR.0000161409.04177.36     Document Type: Article

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