Pendred syndrome: Evidence for genetic homogeneity and further refinement of linkage

Journal of Medical Genetics

Volumn 34, Issue 2, 1997, Pages 126-129

  Gausden, Eleanor ^a   Coyle, Beth ^a   Armour, John A L ^a,i   Coffey, Rebecca ^b   Grossman, Ashley ^c   Fraser, George R ^d   Winter, Robin M ^b   Pembrey, Marcus E ^b   Kendall Taylor, Pat ^e   Stephens, Dafydd ^f   Luxon, Linda M ^g   Phelps, Peter D ^h   Reardon, William ^b   Trembath, Richard ^a  

^a UNIVERSITY OF LEICESTER   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c ST BARTHOLOMEW S HOSPITAL   (United Kingdom)

^d OXFORD UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

^e ROYAL VICTORIA INFIRMARY   (United Kingdom)

^f UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

^g UNIVERSITY COLLEGE LONDON   (United Kingdom)

^h ROYAL NATIONAL THROAT NOSE AND EAR HOSPITAL   (United Kingdom)

ⁱ UNIVERSITY OF NOTTINGHAM   (United Kingdom)

Author keywords

Generic homogeneity; Pendred syndrome; Refinement of linkage

Indexed keywords

IODIDE; MICROSATELLITE DNA; PERCHLORATE; RADIOACTIVE IODINE;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHILD; CHROMOSOMAL LOCALIZATION; CHROMOSOME 7Q; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; GOITER; HAPLOTYPE; HUMAN; HUMAN CELL; MALE; MARKER GENE; PEDIGREE ANALYSIS; PENDRED SYNDROME; PERCEPTION DEAFNESS; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; THYROID FUNCTION;

EID: 16944362537     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.34.2.126     Document Type: Article

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