Associated Papers
Defects in the Mitochondrial Genome of Dogs with Recurrent Tumours.
Kowal K et al.
International Journal of Molecular Sciences, 2024
Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants.
Namjou B et al.
International Journal of Obesity (2005), 2021
Mutation spectrum of TP53 gene predicts clinicopathological features and survival of gastric cancer.
Tahara T et al.
Oncotarget, 2016
27323394 (PubMed )
Supplement: oncotarget-07-42252-s002.xlsx › all_non_silent_mutations_
Analysis of FOXO1 mutations in diffuse large B-cell lymphoma.
Trinh DL et al.
Blood, 2013
Hereditary angioedema in Greek families caused by novel and recurrent mutations.
Speletas M et al.
Human Immunology, 2009
The FANCA gene in Japanese Fanconi anemia: reports of eight novel mutations and analysis of sequence variability.
Tachibana A et al.
Human Mutation, 1999
Mutation at the phenylalanine hydroxylase gene (PAH) and its use to document population genetic variation: the Quebec experience.
Carter KC et al.
European Journal of Human Genetics : Ejhg, 1998
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