Associated Papers
Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type.
Wu J et al.
Frontiers in Genetics, 2022
35368703 (PubMed )
Supplement: DataSheet1.zip › 823861_SupMaterial › Data_Sheet_1.ZIP › raw_datas › patient_2__NGS_raw_data.xlsx › Sheet1
Circulating messenger RNA variants as a potential biomarker for surveillance of hepatocellular carcinoma.
Block T et al.
Frontiers in Oncology, 2022
36582804 (PubMed )
Supplement: Table_2.xlsx › Sheet1
CRTAP variants in early-onset osteoporosis and recurrent fractures.
Costantini A et al.
American Journal of Medical Genetics. Part A, 2017
Next-generation sequencing of common osteogenesis imperfecta-related genes in clinical practice.
Árvai K et al.
Scientific Reports, 2016
Non-Invasive Prenatal Diagnosis of Lethal Skeletal Dysplasia by Targeted Capture Sequencing of Maternal Plasma.
Dan S et al.
Plos One, 2016
27433940 (PubMed )
Supplement: pone.0159355.s014.xls › foetal_gDNA
Nicotine and oxidative stress induced exomic variations are concordant and overrepresented in cancer-associated genes.
Bavarva JH et al.
Oncotarget, 2014
24947164 (PubMed )
Supplement: oncotarget-05-4788-s001.pdf
Allelic background of LEPRE1 mutations that cause recessive forms of osteogenesis imperfecta in different populations.
Pepin MG et al.
Molecular Genetics & Genomic Medicine, 2013
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