• "Mosaic trachea" in a child with trisomy 9 mosaicism
• A case of maternal uniparental disomy of chromosome 9 diagnosed prenatally and the related problem of residual trisomy
• A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9
• A case of partial trisomy 9pter --> q13 due to paternal balanced translocation t (9;21) (q13;q21)
• A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss
• A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell line
• A rare occurrence of three consecutive autosomal trisomic pregnancies in a couple without offspring
• Advances in whole-genome genetic testing: from chromosomes to microarrays
• An infant with trisomy 9 mosaicism presenting as a complete trisomy 9 by amniocentesis
• Another small supernumerary marker chromosome derived from chromosome 9 in a Klinefelter patient
• Antenatal detection of mosaic trisomy 9 by ultrasound: a case report and literature review
• Atypical manifestations of two cases of trisomy 9 syndrome: rethinking development delay
• Birth of a child with trisomy 9 mosaicism syndrome associated with paternal isodisomy 9: case of a positive noninvasive prenatal test result unconfirmed by invasive prenatal diagnosis
• Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosome
• Cardiac Arrest Following Abdominal Catastrophe in a Toddler
• Cardiac Failure in a Trisomy 9 Patient Undergoing Anesthesia: A Case Report
• Case report of a pseudo-isodicentric chromosome 9 resulting in mosaic trisomy 9
• Case report: Detection of fetal trisomy 9 mosaicism by multiple genetic testing methods: Report of two cases
• Characteristics and dental treatment of partial trisomy 9
• Choroid plexus coagulation in trisomy 9 mosaic-related hydrocephalus-a case report
• Choroid plexus hyperplasia and chromosome 9p gains
• Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter
• Chromosomal microarray analysis detects trisomy 9 mosaicism in a prenatal case not revealed by conventional cytogenetic analysis of cord blood
• Chromosomal mosaicism in spontaneous abortions: analysis of 650 cases
• Chromosome abnormalities in a referred population for suspected chromosomal aberrations: a report of 4117 cases
• Chronic myeloid leukemia in chronic phase with a partial trisomy 9 mosaicism
• Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review
• Complex cerebral malformation including Dandy-Walker in a newborn with trisomy 9 mosaicism
• Complex mosaicism associated with trisomy 9
• Confined placental chimerism: prenatal and postnatal cytogenetic and molecular analysis, and pregnancy outcome
• Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization
• Confined placental mosaicism of double trisomies 9 and 21: discrepancy between non-invasive prenatal testing, chorionic villus sampling and postnatal confirmation
• Constitutional mosaicism for a chromosome 9 inversion resulting in recombinant aneusomy in an offspring
• Dental management of a child with trisomy 9 mosaicism: a case report
• Detection of fetal trisomy 9 mosaicism by noninvasive prenatal testing through maternal plasma DNA sequencing
• Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preecl
• Detection of mosaic trisomy 9 missed by conventional cytogenetics using SNP-array and fluorescence in situ hybridization
• Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism
• Distribution of mosaicism in human placentae
• Divergent Levels of Marker Chromosomes in an hiPSC-Based Model of Psychosis
• Establishment of human-embryonic-stem-cell line from mosaic trisomy 9 embryo
• Fetoplacental and fetoamniotic chromosomal discrepancies in prenatally detected mosaic trisomy 9
• First trimester screening for other trisomies than trisomy 21, 18, and 13
• Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature
• Good response to long-term therapy with growth hormone in a patient with 9p trisomy syndrome: A case report and review of the literature
• HELLP syndrome in the 21st week of pregnancy in mosaic trisomy 9
• Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factor
• Homologous recombination of wild-type JAK2, a novel early step in the development of myeloproliferative neoplasm
• Hydrocephalus due to hyperplasia of the choroid plexuses in a patient with trisomy 9 mosaicism. A real diagnostic and therapeutic challenge
• Hypomelanosis Ito in translocation trisomy 9/mosaicism (46,XX/46,XX,t(9;9)(p24;p24)). Spontaneous remission in childhood
• Idiopathic macular hypoplasia: a report of four cases and refinement of the phenotype of so-called ateliotic macula
• Low incidence of UPD in spontaneous abortions beyond the 5th gestational week
• Low-level mosaic trisomy 9 at amniocentesis associated with a positive non-invasive prenatal testing for trisomy 9, maternal uniparental disomy 9, intrauterine growth restriction and a favorable fetal outcome in a pregnancy
• Low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with a favorable fetal outcome, intrauterine growth restriction, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes and perinatal progressive decrease of the
• Misdiagnosis of mosaic tetrasomy 9p in a fetus by single nucleotide polymorphism-based array
• Mosaic tetrasomy 9p at amniocentesis in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the aneuploid cell line and cytogenetic discrepancy in various tissues
• Mosaic trisomy 9 and lobar holoprosencephaly
• Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses
• Mosaic trisomy 9 hematopoietic chimera
• Mosaic trisomy 9 presenting with congenital heart disease, facial dysmorphism and pigmentary skin lesions: intricate issues of genetic counseling
• Mosaic trisomy 9: report of a new case with a long-term survival
• Mosaic Trisomy 9p in a Patient with Mild Dysmorphic Features and Normal Intelligence
• Mosaic vs. nonmosaic trisomy 9: report of a liveborn infant evaluated by fluorescence in situ hybridization and review of the literature
• New report of two patients with mosaic trisomy 9 presenting unusual features and longer survival
• Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p
• Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter- >14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic features
• Pathological findings in the complete trisomy 9 syndrome: three case reports and review of the literature
• Perinatal outcomes of prenatal cases testing positive for trisomy 9 by noninvasive prenatal testing
• PGD for a complex chromosomal rearrangement by array comparative genomic hybridization
• Pitfalls and management of corrective spinal surgery in trisomy 9 mosaicism: a report of three cases
• Prenatal diagnosis and genetic counseling of low-level trisomy 9 mosaicism with a favorable outcome
• Prenatal diagnosis of mosaic trisomy 9
• Prenatal diagnosis of nonmosaic trisomy 9 and related ultrasound findings at 11.7 weeks
• Prenatal diagnosis of nonmosaic trisomy 9 in a fetus with severe renal disease
• Prenatal diagnosis of trisomy 9 mosaic presenting as a case of Dandy-Walker malformation
• Prenatal diagnosis of trisomy 9 mosaicism: two new cases
• Prenatal diagnosis of trisomy 9: cytogenetic, fish, and DNA studies
• Presenting physical characteristics, medical conditions, and developmental status of long-term survivors with trisomy 9 mosaicism
• Rapid confirmation of previously detected prenatal mosaicism by fluorescence in situ hybridization in interphase uncultured amniocytes
• Report of a Case with Trisomy 9 Mosaicism
• Revaluation twenty-three years later of a supernumerary derivative chromosome 9
• SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia
• The reliability of maternal serum triple test in prenatal diagnosis of fetal chromosomal abnormalities of pregnant Turkish women
• The Retinal Pigment Epithelial Cell Line (ARPE-19) Displays Mosaic Structural Chromosomal Aberrations
• Tissue specific mosaicism of trisomy 9 in a patient with severe torsion scoliosis
• Transfusion medicine illustrated: Mosaic Trisomy 9 in an infant with mixed-field ABO blood grouping
• Trisomy 8 detection in Ph+ CML patients using conventional cytogenetic and interphase fluorescence in situ hybridization techniques
• Trisomy 8 in Philadelphia chromosome (Ph1)-negative cells in the course of Ph1-positive chronic myelocytic leukemia
• Trisomy 8: an additional case with unique manifestations [correction]
• Trisomy 9 mosaic syndrome
• Trisomy 9 mosaic syndrome: Sixteen additional patients with new and/or less commonly reported features, literature review, and suggested clinical guidelines
• Trisomy 9 mosaicism and XX sex reversal
• Trisomy 9 mosaicism in a child with a tethered cord
• Trisomy 9 mosaicism in two girls with multiple congenital malformations and mental retardation
• Trisomy 9 mosaicism syndrome. A case report and review of the literature
• Trisomy 9 syndrome: report of a case with Crohn disease and review of the literature
• Trisomy 9: review and report of two new cases
• Twenty-five additional cases of trisomy 9 mosaic: Birth information, medical conditions, and developmental status
• Two patients with trisomy 9 mosaicism
• Varix of the portal vein: prenatal diagnosis in a fetus with mosaic trisomy 9 syndrome