• A case of partial trisomy of chromosome 8p associated with autism
• A child with complementary mosaic trisomy 8 and mosaic trisomy 21; clinical description of Warkany-Down syndrome and mechanism of origin
• A neonate with a unique non-Down syndrome transient proliferative megakaryoblastic disease
• A novel t(8;18)(q13;q21) in acute monocytic leukemia evolving from constitutional trisomy 8 mosaicism
• Aberrations of chromosome 8 in myelodysplastic syndromes: clinical and biological significance
• An unusual case of trisomy 8 mosaicism complicated by coexistence of phenylketonuria
• Anesthetic management of a patient with 8 trisomy mosaic combined with cerebral palsy
• Application of next-generation DNA sequencing for prenatal testing of fetal chromosomal aneuploidies
• Are Duane syndrome and infantile esotropia allelic?
• Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism
• Bilateral severe microphthalmia in a neonate with trisomy 8 mosaicism: A new finding
• Characterization of bone marrow stromal abnormalities in a patient with constitutional trisomy 8 mosaicism and myelodysplastic syndrome
• Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations
• Characterization of trisomic natural killer cell abnormalities in a patient with constitutional trisomy 8 mosaicism
• Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delay
• Chimerism 47,XY, + 8/46,XX: Follow-up for 11 Years
• Chondroid cystic malformation of the lung with trisomy 8 mosaicism: a new cystic lung malformation
• Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter
• Clinical and genetic analysis of a child with mosaic chromosome 8 trisomy syndrome
• Cocaine and trisomy 8 associated with prenatal diagnosis of corpus callosum agenesis
• Coexistence of neurofibromatosis type 1 and mosaic trisomy 8 in the same patient
• Common sonographic characteristics of trisomy 8 mosaicism
• Confined trisomy 8 mosaicism of meiotic origin: a rare cause of aneuploidy in childhood cancer
• Congenital Corneal Opacities Associated With Trisomy 8 Mosaicism Syndrome
• Congenital retinal dystrophy and corneal opacity in trisomy 8 mosaicism
• Constitutional trisomy 8 mosaicism as a model for epigenetic studies of aneuploidy
• Constitutional trisomy 8 mosaicism due to meiosis II non-disjunction in a phenotypically normal woman with hematologic abnormalities
• Constitutional trisomy 8 mosaicism in a healthy bone marrow donor: confirmation of first reported donor origin trisomy 8
• Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies
• Constitutional trisomy 8 mosaicism with myelodysplastic syndrome complicated by intestinal Behcet disease and antithrombin III deficiency
• Constitutional Trisomy 8 Mosaicism with Persistent Macrocytosis
• Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia
• Corneal choristoma associated with trisomy 8 mosaic syndrome: a clinicopathologic report
• Cytogenetic and histological features of a human embryo with homogeneous chromosome 8 trisomy
• Disappearance of the trisomy 8 cell line at long-term follow-up in mosaic trisomy 8 at amniocentesis in a pregnancy with a favorable outcome
• DOUBLE TRISOMY MOSAICISM 48,XXX,+8/46,XX IN A FEMALE: THE FIRST REPORTED CASE
• Duodenal perforation associated with breath stacking and annular pancreas
• Duplication 2p and monosomy 8p in mosaicism: clinical, molecular cytogenetic and molecular markers of a unique case
• Early and Innovative Rehabilitation in Warkany Syndrome 2 Associated with Agenesis of the Corpus Callosum: A Case Report
• Effectiveness of Chromosomal Microarray Analysis for Prenatal Diagnosis of Fetal Echogenic Intracardiac Focus: A Single-Center Experience
• Fetal trisomy 8 mosaicism associated with truncus arteriosus Type I
• First trimester prenatal detection of mosaic trisomy 8
• First trimester screening for other trisomies than trisomy 21, 18, and 13
• Hemihyperplasia and discordant bone age in a patient with trisomy 8 mosaicism
• Hemophagocytosis associated with leukemia: a striking association with juvenile myelomonocytic leukemia
• Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review
• Language development impairment and trisomy 8 mosaicism
• Maternal toxoplasma infection and mosaic trisomy 8 syndrome
• Minimal residual disease and trisomy 8
• Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 associated with congenital hypoplasia of the tongue and review of the literature
• Molecular cytogenetic characterization of two small chromosome 8 derived supernumerary mosaic markers
• Mosaic copy number variation in schizophrenia
• Mosaic double aneuploidy (45,X/47,XX,+8) with aortic dissection
• Mosaic partial pericentromeric trisomy 8 and maternal uniparental disomy in a male patient with autism spectrum disorder
• Mosaic ring chromosome 8: clinical and array-CGH findings in partial trisomy 8
• Mosaic Small Supernumerary Marker Chromosome Derived from Five Discontinuous Regions of Chromosome 8 in a Patient with Neutropenia and Oral Aphthous Ulcer
• Mosaic trisomy (8)(p22 --> pter) in a fetus caused by a supernumerary marker chromosome without alphoid sequences
• Mosaic trisomy 8 and Townes-Brocks syndrome due to a novel SALL1 mutation in the same patient
• Mosaic trisomy 8 detected by fibroblasts cultured of skin
• Mosaic trisomy 8 syndrome with a novel finding of ectopic kidney
• Mosaicism for an ectopic NOR at 8pter and a complex rearrangement of chromosome 8 in a patient with severe psychomotor retardation
• Mosaicism for combined tetrasomy of chromosomes 8 and 18 in a dysmorphic child: a result of failed tetraploidy correction?
• Multiple cardiac abnormalities in a case of non-mosaic trisomy 8
• Musculo-mucous web velum and velopharyngeal dysfunction associated with 8q22.1-22.2 microduplication
• Ophthalmologic observations in a patient with partial mosaic trisomy 8
• Optic disc coloboma and localized chorioretinal defects in constitutional partial trisomy 8 mosaicism
• Partial trisomy 8 mosaicism due to a pseudoisodicentric chromosome 8
• Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells
• Persistence of a monosomic cell line in a fetus with mosaic trisomy 8
• PGD for a complex chromosomal rearrangement by array comparative genomic hybridization
• Piecing together a picture of trisomy 8 mosaicism syndrome
• Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats
• Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive cases
• Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum
• Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review
• Prenatal diagnosis of mosaic trisomy 8q studied by ultrasound, cytogenetics, and array-CGH
• Prenatal diagnosis of trisomy 8 mosaicism
• Prenatal diagnosis of trisomy 8 mosaicism, initially identified by cffDNA screening
• Primary myelofibrosis but not autoimmune myelofibrosis accompanied by Sjögren's syndrome and primary biliary cirrhosis in a patient with trisomy 8 mosaic: a case report and literature review
• Prolonged pancytopenia in a gene therapy patient with ADA-deficient SCID and trisomy 8 mosaicism: a case report
• Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences
• Ring chromosome 8 with mosaic trisomy 8 syndrome in an infant
• Rothmund-Thomson syndrome and osteoma cutis in a patient previously diagnosed as COPS syndrome
• Single cell transcriptome in aneuploidies reveals mechanisms of gene dosage imbalance
• Supernumerary ring chromosome 8: clinical and molecular cytogenetic characterization in a case report
• Surgical Repair of Total Anomalous Pulmonary Venous Connection in a Neonate With Mosaic Trisomy 8
• The epigenetic landscape of aneuploidy: constitutional mosaicism leading the way?
• The incidental discovery of a constitutional trisomy 21 mosaicism in an adult female with myelodysplastic/myeloproliferative neoplasm
• Trisomy 8 in an allogeneic stem cell transplant recipient representative of a donor-derived constitutional abnormality
• Trisomy 8 mosaicism a controversial prenatal diagnosis
• Trisomy 8 mosaicism and favorable outcome after treatment of infantile spasms: case report
• Trisomy 8 Mosaicism in a Boy with Dysmorphic Features
• Trisomy 8 mosaicism in a patient born to a mother with 47,XXX
• Trisomy 8 mosaicism in a patient with heterotaxia
• Trisomy 8 mosaicism in the placenta: A Danish cohort study of 37 cases and a literature review
• Trisomy 8 mosaicism with pyloric atresia and situs ambiguous
• Trisomy 8, a Cytogenetic Abnormality in Myelodysplastic Syndromes, Is Constitutional or Not?
• Upper limb abnormalities in mosaic trisomy 8 syndrome
• Uterus didelphys in mosaic trisomy 8 patient: Management and fertility issues
• Warkany syndrome associated with agenesis of the corpus callosum