• <em>FLT3-ITD</em> signals bad news for core binding factor acute myeloid leukemia unless trisomy 22 comes to the rescue
• 22q13 Microduplication Syndrome in Siblings with Mild Clinical Phenotype: Broadening the Clinical and Behavioral Spectrum
• A pediatric BAL case with double Ph chromosomes and trisomy 5
• A rare case of trisomy 11q23.3-11q25 and trisomy 22q11.1-22q11.21
• Acute myeloid leukemia with inversion of chromosome 16: cytological, immunophenotypic and cytogenetic disruption
• BACs-on-Beads™ assay for a case of trisomy 22 confined placental mosaicism
• BCR/ABL1 fluorescence <em>in situ</em> hybridization fusion signals on both copies of chromosome 22 in a Philadelphia-masked chronic myeloid leukemia case: implication for the therapy
• Chorionic villus cell culture and karyotype analysis in 1 983 cases of spontaneous miscarriage
• Comparison of the etiological constitution of two and three or more recurrent miscarriage
• Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome
• Detection of aneuploidies in spontaneous abortions by quantitative fluorescent PCR with short tandem repeat markers: a retrospective study
• Effects of tyrosine kinase inhibitors for controlling Ph+ clone and additional clonal abnormalities in a chronic myeloid leukemia
• ESOPHAGEAL ATRESIA WITH RECURRENT TRACHEOESOPHAGEAL FISTULAS AND MICRODUPLICATION 22q11.23
• Failure to recombine is a common feature of human oogenesis
• Increased prenatal detection of 22q11.2 deletion and 22q11.2 duplication after introduction of nationwide prenatal screening for trisomy 21, trisomy 13, and trisomy 18
• Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14
• Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion
• Molecular genetic characterization of Philadelphia chromosome-positive acute myeloid leukemia
• MYOCLONIC ASTATIC EPILEPSY IN A PATIENT WITH A DE NOVO 4q21.22q21.23 MICRODUPLICATION
• Non-mosaic trisomy 22 and congenital heart surgery using the shared decision making model: a case report
• Novel method of real-time PCR-based screening for common fetal trisomies
• Occurrence of mosaic trisomy 22 and pericentric inversion of chromosome 9 in a patient with a good prognosis
• Parental balanced chromosomal rearrangement leading to major genomic imbalance and an autosomal trisomy resulting in consecutive pregnancy loss: a case report
• Prenatal diagnosis of low-level trisomy 22 mosaicism with a favorable outcome
• Prenatal diagnosis of trisomy 22 at the first trimester of pregnancy
• Trisomy 22 Mosaicism from Prenatal to Postnatal Findings: A Case Series and Systematic Review of the Literature
• Trisomy 22 with long spina bifida occulta: A case report
• Trisomy 22: First and Second Trimester Cytogenetic Analysis and Phenotypic Presentation in a Series of Seven Cases