Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis

Clinical Endocrinology

Volumn 66, Issue 5, 2007, Pages 695-702

  Tenenbaum Rakover, Yardena ^a,b   Mamanasiri, Sunee ^c   Ris Stalpers, Carrie ^d   German, Alina ^a   Sack, Joseph ^e   Allon Shalev, Stavit ^a,b   Pohlenz, Joachim ^f   Refetoff, Samuel ^c  

^a HAEMEK MEDICAL CENTER   (Israel)

^b TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^c UNIVERSITY OF CHICAGO   (United States)

^d ACADEMIC MEDICAL CENTER   (Netherlands)

^e TEL AVIV UNIVERSITY   (Israel)

^f JOHANNES GUTENBERG UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

IODIDE; PERCHLORATE; TECHNETIUM 99M; THYROID PEROXIDASE;

ADOLESCENT; ADULT; ARTICLE; CHILD; CONGENITAL HYPOTHYROIDISM; FEMALE; FOLLOW UP; GENE MUTATION; GENE SEQUENCE; GENETIC TRAIT; HAPLOTYPE; HUMAN; MALE; NEUROLOGIC DISEASE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; THYROID GLAND;

ADOLESCENT; ADULT; ARABS; CHILD; CHILD, PRESCHOOL; CONGENITAL HYPOTHYROIDISM; CONSANGUINITY; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENETIC SCREENING; HAPLOTYPES; HUMANS; IODIDE PEROXIDASE; ISLAM; ISRAEL; MALE; MUTATION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;

EID: 34247885912     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/j.1365-2265.2007.02804.x     Document Type: Article

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