Associated Papers
A novel mutation in collagen transport protein, MIA3 gene, detected in a patient with clinical symptoms of Ehlers-Danlos hypermobile syndrome.
Junkiert-Czarnecka A et al.
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University, 2023
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.
Schubert SA et al.
British Journal of Cancer, 2017
28742792 (PubMed )
Supplement: bjc2017240x1.docx
Pooled DNA resequencing of 68 myocardial infarction candidate genes in French canadians.
Beaudoin M et al.
Circulation. Cardiovascular Genetics, 2012
22923420 (PubMed )
Supplement: 963165_supplemental_material.pdf
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