Associated Papers
Genetic and Clinical Analyses of the KIZ-c.226C>T Variant Resulting in a Dual Mutational Mechanism.
Sundaresan Y et al.
Genes, 2024
Genetic spectrum in a Canadian cohort of apparently sporadic pheochromocytomas and paragangliomas: New data on multigene panel retesting over time.
Parisien-La Salle S et al.
Clinical Endocrinology, 2022
5'UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia.
Marconi C et al.
Journal of Hematology & Oncology, 2017
28100250 (PubMed )
Supplement: 13045_2016_382_MOESM1_ESM.docx
Phenotypic variation in enhanced S-cone syndrome.
Audo I et al.
Investigative Ophthalmology & Visual Science, 2008
Single-amplicon MSH2 A636P mutation testing in Ashkenazi Jewish patients with colorectal cancer: role in presurgical management.
Guillem JG et al.
Annals of Surgery, 2007
Analysis of mutation spectra in UVB-exposed mouse skin epidermis and dermis: frequent occurrence of C-->T transition at methylated CpG-associated dipyrimidine sites.
Ikehata H et al.
Environmental and Molecular Mutagenesis, 2003
A novel nucleolar G-protein conserved in eukaryotes.
Park JH et al.
Journal of Cell Science, 2001
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