• 12q14 microduplication: a new clinical entity reciprocal to the microdeletion syndrome?
• 9p partial monosomy and disorders of sex development: review and postulation of a pathogenetic mechanism
• A 46,XY Female with a 9p24.3p24.1 Deletion and a 8q24.11q24.3 Duplication: A Case Report and Review of the Literature
• A case of 9p deletion syndrome with Duane retraction syndrome
• A case of 9p partial monosomy syndrome
• A de novo unbalanced translocation leading to partial monosomy 9p23-pter and partial trisomy 15q25.3-qter associated with 46,XY complete gonadal dysgenesis, tall stature and mental retardation
• A Meta-Analysis Evaluating Clinical Outcomes of Patients with Renal Cell Carcinoma Harboring Chromosome 9P Loss
• 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)
• Allelic loss of 9p21.3 is a prognostic factor in 1p/19q codeleted anaplastic gliomas
• Analysis of a pedigree with partial trisomy 9 and partial monosomy 13 derived from a maternal balanced t(9;13) translocation
• Analysis of ring chromosome 9 syndrome with fluorescence in situ hybridization
• Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH
• Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation
• Case report. Familial balanced translocation leading to an offspring with phenotypic manifestations of 9p syndrome
• Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q
• Chromosomal deletion of 9p21 is linked to poor patient prognosis in papillary and clear cell kidney cancer
• Chromosome 9p deletion in clear cell renal cell carcinoma predicts recurrence and survival following surgery
• Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions
• Chromosome 9P deletion: Gonadal dysgenesis associated with mental retardation and hypoplasia of the corpus callosum: A contiguous gene syndrome?
• Chromosome 9p deletions are an independent predictor of tumor progression following nephrectomy in patients with localized clear cell renal cell carcinoma
• Chromosome 9p deletions identify an aggressive phenotype of clear cell renal cell carcinoma
• Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype
• Clinical and neuroradiological features of the 9p deletion syndrome
• Clinical findings and molecular cytogenetic study of de novo pure chromosome 9p deletion: Pre- and postnatal diagnosis
• Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11
• Coexistence of 9p Deletion Syndrome and Autism Spectrum Disorder
• Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion
• Complex chromosome rearrangement 46,XY, der(9)t(Y;9)(q12;p23) in a girl with sex reversal and mental retardation
• Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature
• Contrast enhancement in 1p/19q-codeleted anaplastic oligodendrogliomas is associated with 9p loss, genomic instability, and angiogenic gene expression
• Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene
• Cytogenetic and array-CGH characterization of a complex de novo rearrangement involving duplication and deletion of 9p and clinical findings in a 4-month-old female
• Cytogenetic and prognostic analysis in adult patients with Philadelphia chromosome-positive and bcr-abl positive acute lymphoblastic leukaemia
• Cytogenetic profile predicts prognosis of patients with clear cell renal cell carcinoma
• Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype
• Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9p
• Developmental glaucoma with chromosomal abnormalities of 9p deletion and 13q duplication
• Downregulation of NDUFB6 due to 9p24.1-p13.3 loss is implicated in metastatic clear cell renal cell carcinoma
• Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism
• Duplication 9p and their implication to phenotype
• Entire FGF12 duplication by complex chromosomal rearrangements associated with West syndrome
• Genetic analysis of a case with a supernumerary marker derived from chromosome 9
• Genetic analysis of a family with 9q34.3 microdeletion and microduplication caused by abnormal chromosome balance structure
• Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesis
• Genetic study of a fetus with 9p direct duplication deletion syndrome
• Genomic aberrations in 80 cases of primary glioblastoma multiforme: Pathogenetic heterogeneity and putative cytogenetic pathways
• High-resolution array copy number analyses for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors: four cases of homozygous deletions of the CDKN2A gene
• Hypodiploidy has unfavorable impact on survival in pediatric acute myeloid leukemia: an I-BFM Study Group collaboration
• Identification of a possible association of JAK2 in development of microphthalmia, anophthalmia, and coloboma (MAC) complex in a child with 9p deletion and duplication
• Impact of 9p deletion and p16, Cyclin D1, and Myc hyperexpression on the outcome of anaplastic oligodendrogliomas
• Independent post-zygotic breaks of a dicentric chromosome result in mosaicism for an inverted duplication deletion 9p and terminal deletion 9p
• Inherited deletion of 9p22.3-p24.3 and duplication of 18p11.31-p11.32 associated with neurodevelopmental delay: Phenotypic matching of involved genes
• Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature Review
• Integrated Genomics for Pinpointing Survival Loci within Arm-Level Somatic Copy Number Alterations
• Investigation of the candidate region for trigonocephaly in a patient with monosomy 9p syndrome using array-CGH
• Loss of 9p21 Regulatory Hub Promotes Kidney Cancer Progression by Upregulating HOXB13
• Losses at chromosome 4q are associated with poor survival in operable ductal pancreatic adenocarcinoma
• Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization
• miR-101 DNA copy loss is a prominent subtype specific event in lung cancer
• Molecular cytogenetic characterization of a de novo derivative chromosome X with an unbalanced t(X;9) translocation in a fetus and literature review
• Molecular genetic analysis of partial 9p trisomy in two Chinese families with mental retardation and facial anomaly
• Monosomy 9p24 in two non-related patients as result of a translocation (2;9)
• Mosaic distal 9p deletion or 46,XY,del(9)(p23)/46,XY at amniocentesis in a pregnancy associated with perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome
• Mutation status of K-ras, p53 and allelic losses at 9p and 18q are not prognostic markers in patients with pancreatic cancer
• Neonatal hyperinsulinemic hypoglycemia in a patient with 9p deletion syndrome
• Normal intelligence and premature ovarian failure in an adult female with a 7.6 Mb de novo terminal deletion of chromosome 9p
• Novel chromosomal translocation t(11;9)(p15;p23) involving deletion and duplication of 9p in a girl associated with autism and mental retardation
• Partial deletion 9p syndrome in Malaysian children
• Partial monosomy 9p (9p22.2-->pter) and partial trisomy 18q (18q21.32-->qter) in a female infant with anorectal malformations
• Partial trisomy 4q and partial monosomy 9p in a girl with choanal atresia and various dysmorphic findings
• Partial trisomy 9p and partial monosomy 7p of an infant inherited from maternal balanced translocation: a case report
• Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl
• Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family
• Patient with terminal 9 Mb deletion of chromosome 9p: refining the critical region for 9p monosomy syndrome with trigonocephaly
• Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly
• Polymicrogyria in a child with inv dup del(9p) and 22q11.2 microduplication
• Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions
• Precise breakpoint detection in a patient with 9p- syndrome
• Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review
• Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication
• Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in a fetus with major congenital anomalies
• Prenatal diagnosis of a female fetus with ring chromosome 9, 46,XX,r(9)(p24q34), and a de novo interstitial 9p deletion
• Prenatal diagnosis of de novo isochromosome 4p with an unbalanced t(4;9) translocation in a fetus with congenital anomalies: A case report and literature review
• Pure distal 9p deletion in a female infant with cerebral palsy
• Reciprocal chromosome translocations involving short arm of chromosome 9 as a risk factor of unfavorable pregnancy outcomes after meiotic malsegregation 2:2
• Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome
• Ring Chromosome 9 and Chromosome 9p Deletion Syndrome in a Patient Associated with Developmental Delay: A Case Report and Review of the Literature
• Ring chromosome 9 in a girl with developmental delay and dysmorphic features: case report and review of the literature
• Ring chromosome formation by intra-strand repairing of subtelomeric double stand breaks and clinico-cytogenomic correlations for ring chromosome 9
• Risk prediction for metastasis of clear cell renal cell carcinoma using digital multiplex ligation-dependent probe amplification
• Sex discordance identification following non-invasive prenatal testing
• Simultaneous 9p Deletion and 8p Duplication in a Seven-Year-Old Girl, Detected Using Multiplex Ligation-Dependent Probe Amplification: A Case Report
• Subtelomeric fish findings in Turkish patients with idiopathic mental retardation
• Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients
• Three unrelated patients with congenital anterior pituitary aplasia and a characteristic physical and neuropsychological phenotype: a new syndrome?
• Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p
• Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays
• Unusual Chromosomal Rearrangement Resulted in Interstitial Monosomy 9p: Case Report
• Using a new analytic approach for genotyping and phenotyping chromosome 9p deletion syndrome
• Whole Genome Sequencing Reveals a Chromosome 9p Deletion Causing DOCK8 Deficiency in an Adult Diagnosed with Hyper IgE Syndrome Who Developed Progressive Multifocal Leukoencephalopathy