Associated Papers
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37372431 (PubMed )
Supplement: genes-14-01251-s001.zip › HGV__3.xlsx › _3
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome.
Smyk M et al.
Genes, 2023
36980952 (PubMed )
Supplement: genes-14-00680-s001.zip › Supplementary_Table_S5.xlsx › Arkusz1
Whole-Genome Profiles of Malay Colorectal Cancer Patients with Intact MMR Proteins.
Juhari WKW et al.
Genes, 2021
A glioneuronal tumor with CLIP2-MET fusion.
Chowdhury T et al.
Npj Genomic Medicine, 2020
32550005 (PubMed )
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Molecular Guided Therapy Provides Sustained Clinical Response in Refractory Choroid Plexus Carcinoma.
Cornelius A et al.
Frontiers in Pharmacology, 2017
28993730 (PubMed )
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A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy.
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Plos One, 2013
24358150 (PubMed )
Supplement: pone.0082154.s002.xls › Sheet1
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