Pendred's syndrome: Identification of the genetic defect a century after its recognition

Thyroid

Volumn 9, Issue 1, 1999, Pages 65-69

  Kopp, Peter ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 7Q; CLINICAL ARTICLE; GENE LOCUS; GENE MUTATION; HUMAN; PENDRED SYNDROME; PRIORITY JOURNAL; REVIEW; THYROID FOLLICLE;

EID: 0033062827     PISSN: 10507256     EISSN: None     Source Type: Journal    
DOI: 10.1089/thy.1999.9.65     Document Type: Review

References (47)

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