The deleted in colorectal carcinoma (DCC) gene 201 R→G polymorphism: No evidence for genetic association with autoimmune disease

European Journal of Human Genetics

Volumn 11, Issue 11, 2003, Pages 840-844

  Hall, Richard J ^a   Merriman, Marilyn E ^a   Green, Rachel A ^a   Markham, Valerie H ^a   Smyth, Deborah J ^b   Heward, Joanne M ^c   Jennings, Claire E ^d   Braithwaite, Antony W ^a   Cundy, Tim ^e   Darlow, Brian A ^f   Gow, Peter J ^g   Harrison, Andrew A ^h   Highton, John ^a   Hunt, Penny J ^f   Manning, Patrick ⁱ   Pokorny, Violetta ^e   Scott, Russell S ^j   Taylor, Barry J ⁱ   Willis, Jinny A ^j   Yeoman, Sue ^k   McLean, Lachy ^e   Gough, Stephen C L ^c   Pearce, Simon H ^d   Merriman, Tony R ^a   more..

^a UNIVERSITY OF OTAGO   (New Zealand)

^b ADDENBROOKE S HOSPITAL   (United Kingdom)

^c BIRMINGHAM HEARTLANDS HOSPITAL   (United Kingdom)

^d NEWCASTLE UNIVERSITY   (United Kingdom)

^e UNIVERSITY OF AUCKLAND   (New Zealand)

^f CHRISTCHURCH HOSPITAL   (New Zealand)

^g MIDDLEMORE HOSPITAL   (New Zealand)

^h UNIVERSITY OF OTAGO   (New Zealand)

ⁱ DUNEDIN HOSPITAL   (New Zealand)

^j Lipid and Diabetes Research Group   (New Zealand)

^k AUCKLAND CITY HOSPITAL   (New Zealand)

more..

Author keywords

Autoimmunity; DCC; Genetic association; IDDM6; Polymorphism

Indexed keywords

CYTOSINE; DNA; GUANINE; IMMUNOGLOBULIN; NUCLEOTIDE;

ADOLESCENT; ADULT; APOPTOSIS; ARTICLE; AUTOIMMUNE DISEASE; AUTOIMMUNITY; CASE CONTROL STUDY; CHILD; CHROMOSOME 18Q; COHORT ANALYSIS; COLORECTAL CARCINOMA; CONTROLLED STUDY; DNA POLYMORPHISM; GENE DELETION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENETIC SCREENING; GRAVES DISEASE; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; MAJOR CLINICAL STUDY; NEW ZEALAND; PHENOTYPE; PRIORITY JOURNAL; RHEUMATOID ARTHRITIS; TUMOR SUPPRESSOR GENE; UNITED KINGDOM;

ADULT; AGE OF ONSET; AUTOIMMUNE DISEASES; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; COLORECTAL NEOPLASMS; GENES, DCC; GENETICS, POPULATION; HAPLOTYPES; HETEROZYGOTE; HUMANS; MICROSATELLITE REPEATS; POLYMORPHISM, GENETIC;

EID: 10744220601     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201059     Document Type: Article

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