Disease: Chromosome 10- uniparental disomy of
- Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype
- Comparative genome-wide profiling of post-transplant lymphoproliferative disorders and diffuse large B-cell lymphomas
- Fetal Megalencephaly with Cortical Dysplasia at 18 Gestational Weeks Related to Paternal UPD Mosaicism with <em>PTEN</em> Mutation
- First case report of complete paternal isodisomy of chromosome 10 harbouring a novel variant in COL17A1 that causes junctional epidermolysis bullosa intermediate
- Genome-wide genetic characterization of an atypical meningioma by single-nucleotide polymorphism array-based mapping and classical cytogenetics
- Genomic Analyses of Patients With Unexplained Early-Onset Scoliosis
- Identification of maternal uniparental isodisomy of chromosome 10 in a patient with mitochondrial DNA depletion syndrome
- Loss of heterozygosity and uniparental disomy of chromosome region 10q23.3-26.3 in glioblastoma
- Molecular analyses of glioblastoma stem-like cells and glioblastoma tissue
- Molecular cytogenetic analysis of chromosomal aberrations in cells of low grade gliomas and its contribution for tumour classification
- Mosaicism trisomy 10 in a 14-month-old child with additional neurological abnormalities: case report and literature review
- Novel mutation of the perforin gene and maternal uniparental disomy 10 in a patient with familial hemophagocytic lymphohistiocytosis
- Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation
- Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results
- Trisomy 10 mosaicism and maternal uniparental disomy 10 in a liveborn infant with severe congenital malformations