• "Molecular rulers" for calibrating phenotypic effects of telomere imbalance
• 10q26.1 Microdeletion: Redefining the critical regions for microcephaly and genital anomalies
• 5q11, 8p11, and 10q22 are recurrent chromosomal breakpoints in prostate cancer cell lines
• A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature
• A novel interstitial deletion of 10q24.2q24.32 in a patient with renal coloboma syndrome
• A PATIENT WITH PARTIAL CHROMOSOME 12q DUPLICATION AND 10q DELETION
• A Patient with Trisomy 4p and Monosomy 10q
• A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26)
• A subterminal deletion of the long arm of chromosome 10: a clinical report and review
• Altered expression of MGMT in high-grade gliomas results from the combined effect of epigenetic and genetic aberrations
• An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma
• Analysis of PTEN mutations and deletions in B-cell non-Hodgkin's lymphomas
• Association of chromosome 10 losses and negative prognosis in oligoastrocytomas
• Bilateral cryptorchidism associated with terminal deletion of 10q
• Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature
• Chromosomal 10Q26 trisomy resulting from paternal T(9;10)(PTER;Q26.1)
• Chromosome 10q deletion del (10)(q26.1q26.3) is associated with cataract
• Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patients
• Clinical and genetic characterization of patients with Pierre Robin sequence and spinal disease: review of the literature and novel terminal 10q deletion
• Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial monosomy 3p and partial trisomy 10q in human
• Clinical significance of chromosome 8p, 10q, and 16q deletions in prostate cancer
• Comparative genomic hybridization detects specific cytogenetic abnormalities in pediatric ependymomas and choroid plexus papillomas
• Complex distal 10q rearrangement in a girl with mild intellectual disability: follow up of the patient and review of the literature of non-acrocentric satellited chromosomes
• Congenital indifference to pain and deletion of chromosome 10q-: new association
• Correlation of histology and molecular genetic analysis of 1p, 19q, 10q, TP53, EGFR, CDK4, and CDKN2A in 91 astrocytic and oligodendroglial tumors
• Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?
• Cytogenetic aberrations in perineurioma: variation with subtype
• Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient
• Deciphering the complexity of the 4q and 10q subtelomeres by molecular combing in healthy individuals and patients with facioscapulohumeral dystrophy
• Deletion of 2q37 and duplication of 10q24: two cases in the same family and review of the literature
• Deletion of chromosome 10q--a marker for metastasis of head-neck carcinomas?
• Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases
• Distal 10q monosomy: new evidence for a neurobehavioral condition?
• Distal 10q trisomy associated with bilateral hydronephrosis in infancy
• Distal trisomy 10q/partial monosomy 14q: an unusual clinical picture
• Distal trisomy of 10q with distal monosomy of 15q due to a paternal translocation
• Dual MGMT inactivation by promoter hypermethylation and loss of the long arm of chromosome 10 in glioblastoma
• Early renal insufficiency in a neonate with de novo partial trisomy of chromosome 10q
• Evidence-Based Diagnostic Algorithm for Glioma: Analysis of the Results of Pathology Panel Review and Molecular Parameters of EORTC 26951 and 26882 Trials
• Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet
• Familial complex 3q;10q rearrangement unraveled by subtelomeric FISH analysis
• Fine mapping of chromosome 10q deletions in mycosis fungoides and sezary syndrome: identification of two discrete regions of deletion at 10q23.33-24.1 and 10q24.33-25.1
• Fine-structure deletion mapping of 10q22-24 identifies regions of loss of heterozygosity and suggests that sporadic follicular thyroid adenomas and follicular thyroid carcinomas develop along distinct neoplastic pathways
• Fluorescence in situ hybridization (FISH) evaluation of chromosomes 6, 7, 9 and 10 throughout human melanocytic tumorigenesis
• Gardner-Silengo-Wachtel or genito-palato-cadiac syndrome with associated autosomal aneuploidy
• Genetic Alterations in Gliosarcoma and Giant Cell Glioblastoma
• Genetic evidence for a novel gene(s) involved in urogenital development on 10q26
• Genomic alterations in low-grade, anaplastic astrocytomas and glioblastomas
• Genomic changes in primary lesion and lymph node metastases of esophageal squamous cell carcinoma
• Homozygous PTEN deletion in neuroblastoma arising in a child with Cowden syndrome
• Identification of critical regions for clinical features of distal 10q deletion syndrome
• Interstitial deletion of 10q23.1 and confirmation of three 10qdel syndromes
• Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements
• Juvenile polyposis of infancy associated with paracentric inversion and deletion of chromosome 10 in a Hispanic patient: a case report
• Long arm deletion of chromosome 10 in a boy with monorchidism
• Loss of a small region around the PTEN locus is a major chromosome 10 alteration in prostate cancer xenografts and cell lines
• miR-146b-5p inhibits glioma migration and invasion by targeting MMP16
• Molecular analysis of anaplastic oligodendroglial tumors in a prospective randomized study: A report from EORTC study 26951
• Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion
• Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development
• Molecular genetic analysis of ependymal tumors. NF2 mutations and chromosome 22q loss occur preferentially in intramedullary spinal ependymomas
• Monosomy of chromosome 10q26 with mild psychomotor retardation: report of one case
• New corneal findings in chromosome 10 deletion syndrome: report of two cases of corneal ectasia of varying severity
• Novel Finding of Copy Number Gains in GNAS and Loss of 10q in a Child With Malignant Transformation of Neurocutaneous Melanosis Syndrome
• Novel interstitial deletion of 10q24.3-25.1 associated with multiple congenital anomalies including lobar holoprosencephaly, cleft lip and palate, and hypoplastic kidneys
• Novel Unbalanced Translocations Affecting the Long Arms of Chromosomes 10 and 22 Cause Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy
• On the significance of craniosynostosis in a case of Kabuki syndrome with a concomitant KMT2D mutation and 3.2 Mbp de novo 10q22.3q23.1 deletion
• Partial duplication of 3q and distal deletion of 10q inherited from a maternal balanced translocation
• Partial monosomy of distal 10q: three new cases and a review
• Partial trisomy 10q (10q25.1 →qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization
• Patients with high-grade gliomas harboring deletions of chromosomes 9p and 10q benefit from temozolomide treatment
• Persistence of müllerian duct structures in a genetic male with distal monosomy 10q
• Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia
• Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion
• Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects
• Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter)
• Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results
• Prenatal diagnosis of partial trisomy 10q (10q25.3-->qter) and partial monosomy 18q (18q23-->qter)
• Private rare deletions in SEC16A and MAMDC4 may represent novel pathogenic variants in familial axial spondyloarthritis
• Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence
• Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes
• Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities
• Recurrent unbalanced whole-arm t(1;10)(q10;p10) in myelodysplastic syndrome: a case report and literature review
• Relevance of PTEN loss in brain metastasis formation in breast cancer patients
• Ring chromosome 10: report on two patients and review of the literature
• Sacrococcygeal teratoma in a fetus with prenatally diagnosed partial trisomy 10q (10q24.3-->qter) and partial monosomy 17p (p13.3-->pter)
• Severe musculoskeletal phenotype associated with an unbalanced t(6;10) translocation: clarification of the locus for this phenotype on distal 6p
• Significance of a prenatally diagnosed del(10)(q23)
• Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
• Terminal deletion of chromosome 10q at band 26.1: follow-up in an adolescent male with high-output renal failure from congenital obstructive uropathy
• Terminal deletion of chromosome 10q: clinical features and literature review
• Terminal deletion of chromosome 10q26: delineation of two clinical phenotypes
• Terminal deletion of the long arm of chromosome 10
• The chromosome 10 monosomy common in human melanomas results from loss of two separate tumor suppressor loci
• The chromosome 10q26 susceptibility locus in age-related macular degeneration
• The Genomics of Prostate Cancer: emerging understanding with technologic advances
• Two concurrent chromosomal aberrations involving interstitial deletion in 1q24.2q25.2 and inverted duplication and deletion in 10q26 in a patient with stroke associated with antithrombin deficiency and a patent foramen ovale
• Urinary retention in a boy with terminal deletion of chromosome 10q at band 26.1
• WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome
• Woman with UV hypersensitivity and a de novo unbalanced chromosome translocation