Further indications for genetic heterogeneity of euthyroid familial goiter

Journal of Molecular Medicine

Volumn 81, Issue 11, 2003, Pages 736-745

  Neumann, Susanne ^a   Bayer, Yvonne ^a   Reske, Andreas ^a   Tajtáková, Mária ^b   Langer, Pavel ^c   Paschke, Ralf ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

^b P J AFÁRIK UNIVERSITY   (Slovakia)

^c INSTITUTE OF EXPERIMENTAL ENDOCRINOLOGY   (Slovakia)

Author keywords

Candidate loci; Euthyroid goiter; Genetic predisposition; Genotyping; Linkage analysis

Indexed keywords

CARRIER PROTEIN; PENDRIN; SODIUM IODINE SYMPORTER; THYROGLOBULIN; THYROID PEROXIDASE; THYROTROPIN RECEPTOR; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; CHILD; CHROMOSOMAL LOCALIZATION; CLINICAL FEATURE; CONTROLLED STUDY; EUTHYROID FAMILIAL GOITER; FAMILIAL DISEASE; FAMILY STUDY; FEMALE; GENE IDENTIFICATION; GENE LOCATION; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC PREDISPOSITION; GERM LINE; GOITER; HAPLOTYPE; HEARING IMPAIRMENT; HUMAN; IODINE DEFICIENCY; MAJOR CLINICAL STUDY; MALE; MICROSATELLITE MARKER; PEDIGREE ANALYSIS; SCORING SYSTEM; TWINS;

ADOLESCENT; ADULT; AGE OF ONSET; AGED; CHILD; FAMILY; FEMALE; GENETIC MARKERS; GOITER; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; PEDIGREE; THYROID NODULE;

EID: 0345375966     PISSN: 09462716     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00109-003-0463-6     Document Type: Article

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