A comprehensive screen for SNP associations on chromosome region 5q31-33 in Swedish/Norwegian celiac disease families

European Journal of Human Genetics

Volumn 15, Issue 9, 2007, Pages 980-987

  Amundsen, Silja Svanstrøm ^a   Adamovic, Svetlana ^b   Hellqvist, Åsa ^b   Nilsson, Staffan ^c,d   Gudjónsdóttir, Audur H ^e   Ascher, Henry ^e,f   Ek, Johan ^g   Larsson, Kristina ^h   Wahlström, Jan ^b   Lie, Benedicte A ⁱ   Sollid, Ludvig M ^a,i   Naluai, Åsa Torinsson ^b,d  

^a UNIVERSITY OF OSLO   (Norway)

^b UNIVERSITY OF GOTHENBURG   (Sweden)

^c CHALMERS UNIVERSITY OF TECHNOLOGY   (Sweden)

^d UNIVERSITY OF GOTHENBURG   (Sweden)

^e QUEEN SILVIA CHILDREN'S HOSPITAL   (Sweden)

^f NORDIC SCHOOL OF PUBLIC HEALTH   (Sweden)

^g Buskerud Central Hospital   (Norway)

^h UPPSALA UNIVERSITY   (Sweden)

ⁱ OSLO UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

HLA DQ ANTIGEN;

ARTICLE; CELIAC DISEASE; CHROMOSOME 5Q; CHROMOSOME ANALYSIS; COHORT ANALYSIS; FAMILY STUDY; GENE DUPLICATION; GENE IDENTIFICATION; GENE NUMBER; GENETIC ASSOCIATION; GENETIC CODE; GENETIC LINKAGE; GENETIC RISK; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; NORWAY; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RISK ASSESSMENT; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; SWEDEN; UNINDEXED SEQUENCE;

CELIAC DISEASE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 5; COHORT STUDIES; GENETIC SCREENING; GENOTYPE; HAPLOTYPES; HUMANS; NORWAY; POLYMORPHISM, SINGLE NUCLEOTIDE; QUALITY CONTROL; SWEDEN;

EID: 34548150721     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201870     Document Type: Article

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