• "Facilitated consensus," "ethics facilitation," and unsettled cases
• A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
• A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome
• A four-vessel umbilical cord with omphalomesenteric duct in trisomy 18
• A patient with hypopituitarism and isochromosome 18q mosaicism
• An infant with trisomy 18 and a ventricular septal defect
• Anesthetic management for laparoscopic Nissen fundoplication in a 18 trisomy patient with congestive heart disease
• Application of different technologies for distinguishing true and pseudo mosaicisms during prenatal diagnosis
• Beyond the first trimester screen: can we predict who will choose invasive testing?
• Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature
• Cell-free fetal DNA and maternal serum analytes for monitoring embryonic and fetal status
• Chromosome abnormalities and congenital heart diseases: a retrospective on 49 cases
• Chromosome-selective sequencing of maternal plasma cell-free DNA for first-trimester detection of trisomy 21 and trisomy 18
• Clinical courses of trisomy 18 (Edwards syndrome) - an update
• Clinical experience of noninvasive prenatal testing with cell-free DNA for fetal trisomies 21, 18, and 13, in a general screening population
• Co-occurrence of mosaic supernumerary isochromosome 18p and intermittent 2q13 deletions in a child with multiple congenital anomalies
• Commentary on "Consensus, clinical decision making, and unsettled cases"
• Complete and pure trisomy 18p due to a complex chromosomal rearrangement in a male adult with mild intellectual disability
• Confronting ambiguity: identifying options for infants with trisomy 18
• Consensus, clinical decision making, and unsettled cases
• Development of multiple quantitative fluorescent PCR for rapid diagnosis of common aneuploidy and it's clinical application
• Different conformation of two supernumerary 18p isochromosomes, one with a concomitant partial 18q trisomy
• Ethical challenges posed by trisomy 18 infants
• External Quality Assessment for Detection of Fetal Trisomy 21, 18, and 13 by Massively Parallel Sequencing in Clinical Laboratories
• Familial 18p deletion syndrome and 18p partial trisomy inherited from a mother with balanced translocation
• First-trimester screening for trisomy 21 in Denmark: implications for detection and birth rates of trisomy 18 and trisomy 13
• From pediatric history. Important personalities in relation to some genetic defects - "trisomies"
• Gene expression analysis of amniotic fluid: new biomarkers and novel antenatal treatments
• Hyaline vascular Castleman's disease representing 18 trisomy
• Identification and characterization of three inherited genomic copy number variations associated with familial schizophrenia
• Individualized correction for maternal weight in calculating the risk of chromosomal abnormalities with first-trimester screening data
• Inpatient hospital care of children with trisomy 13 and trisomy 18 in the United States
• Major chromosomal anomalies among very low birth weight infants in the Vermont Oxford Network
• Maternal serum IGF-I, IGFBP-1 and IGFBP-3 at 11-13 weeks in trisomy 21 and trisomy 18 pregnancies
• Maximal amniotic fluid index as a prognostic factor in pregnancies complicated by polyhydramnios
• Metabolomic analysis for first-trimester trisomy 18 detection
• Molecular genetic analysis reveals atypical confined placental mosaicism with a small supernumerary marker chromosome derived from chromosome 18: A clinical report of discordant results from three prenatal tests
• Morphological evaluation of lateral ventricles of fetuses with ventriculomegaly by three-dimensional ultrasonography and magnetic resonance imaging: correlation with etiology
• Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18
• Noninvasive prenatal diagnosis of trisomy 21, 18 and 13 using cell-free fetal DNA
• Noninvasive prenatal testing for aneuploidy-ready for prime time?
• Noninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester population
• Outcomes of cardiac surgery in trisomy 18 patients
• Paper 4: EUROCAT statistical monitoring: identification and investigation of ten year trends of congenital anomalies in Europe
• Partial tetrasomy 18 mosaicism: Pre and postnatal diagnosis of a unique pattern
• Performance of different methods of estimating risk screening for chromosomal anomalies
• Phenotypic and genetic analysis of a boy with a 10p15.3 deletion and partial trisomy 18p syndrome
• Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies
• Prenatal diagnosis of de novo partial trisomy 18p and partial monosomy 18q recurrent in a family with fatal aortic coarctation
• Prenatal diagnosis of mobile flap-like tissue on the ventricular septal defect in a newborn with trisomy 18
• Prenatal diagnosis of mosaic tetrasomy 18p
• Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associations
• Rapid diagnosis of aneuploidy by high-resolution melting analysis of segmental duplications
• Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe
• Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversion
• Secondary findings from non-invasive prenatal testing for common fetal aneuploidies by whole genome sequencing as a clinical service
• Tetrasomy 18p in a child with trisomy 18 phenotype
• The experience of families with children with trisomy 13 and 18 in social networks
• The role of the clinical ethics consultant in "unsettled" cases
• Thymic-thoracic ratio in fetuses with trisomy 21, 18 or 13
• Transcriptomic analysis of cell-free fetal RNA suggests a specific molecular phenotype in trisomy 18
• Trisomy 18: how far should we go
• Trisomy 18p caused by a supernumerary marker with a chromosome 13/21 centromere: a possible recurrent chromosome aberration
• Two-Generation Transmission of Trisomy 18p: Prenatal Diagnosis in a Woman with Mild Intellectual Disability