Associated Papers
EVALUATION OF AGREEMENT BETWEEN C/T-13910 POLYMORPHISM GENOTYPING RESULTS AND LACTOSE TOLERANCE TEST RESULTS: A RETROSPECTIVE POPULATION-BASED STUDY IN BRAZIL.
Cavichio MWE et al.
Arquivos De Gastroenterologia, 2024
Pilot study of correlation of selected genetic factors with cribra orbitalia in individuals from a medieval population from Slovakia.
Bľandová G et al.
International Journal of Paleopathology, 2023
Array genotyping as diagnostic approach in medical genetics.
Witsch-Baumgartner M et al.
Molecular Genetics & Genomic Medicine, 2022
35912641 (PubMed )
Supplement: MGG3-10-e2016-s001.docx
The hazards of genotype imputation in chromosomal regions under selection: A case study using the Lactase gene region.
Ali AT et al.
Annals of Human Genetics, 2022
Lactose malabsorption is a risk factor for decreased bone mineral density in pancreatic insufficient cystic fibrosis patients.
Mądry E et al.
European Journal of Human Genetics : Ejhg, 2012
Mild CFTR mutations and genetic predisposition to lactase persistence in cystic fibrosis.
Mądry E et al.
European Journal of Human Genetics : Ejhg, 2011
Adult-type hypolactasia and lactose malabsorption in Poland.
Mądry E et al.
Acta Biochimica Polonica, 2010
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