• Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism
• Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability
• BACs-on-Beads™ assay for a case of trisomy 22 confined placental mosaicism
• Chorionic villus cell culture and karyotype analysis in 1 983 cases of spontaneous miscarriage
• Chromosomal segregation in sperm of the Robertsonian translocation (21;22) carrier and its impact on IVF outcome
• Comparison of the etiological constitution of two and three or more recurrent miscarriage
• Fetal aneuploidy screening by maternal plasma DNA sequencing: 'false positive' due to confined placental mosaicism
• Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts
• Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14
• Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review
• Mosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case report
• Non-invasive prenatal testing to detect chromosome aneuploidies in 57,204 pregnancies
• Non-mosaic trisomy 22 and congenital heart surgery using the shared decision making model: a case report
• Pregnancy outcome of autosomal aneuploidies other than common trisomies detected by noninvasive prenatal testing in routine clinical practice
• Prenatal diagnosis of low-level trisomy 22 mosaicism with a favorable outcome
• Trisomy 22 mosaicism and normal developmental outcome: report of two patients and review of the literature
• Trisomy 22 Mosaicism from Prenatal to Postnatal Findings: A Case Series and Systematic Review of the Literature
• Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmata
• Trisomy 22 with long spina bifida occulta: A case report