• 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 9p13-->p24 duplication coupled with a whole 22q translocation onto 9p24
• A case of partial trisomy 9pter --> q13 due to paternal balanced translocation t (9;21) (q13;q21)
• A complex association of cardiomyopathy, mild dysmorphisms and leukoencephalopathy
• A de novo chromosome 9p duplication in a female child with short stature and developmental delay
• A de novo cryptic 5p deletion and 9p duplication detected by subtelomeric MLPA in a boy with cri du chat syndrome
• A de novo partial trisomy 9p with Dandy-Walker malformation and ventriculomegaly
• 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 fetus with trisomy 9p and trisomy 10p originating from unbalanced segregation of a maternal complex chromosome rearrangement t(4;10;9)
• A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): a case report
• 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)
• Analysis of a pedigree with partial trisomy 9 and partial monosomy 13 derived from a maternal balanced t(9;13) translocation
• 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
• Array-CGH study of partial trisomy 9p without mental retardation
• Association of partial trisomy 9p and the Dandy-Walker malformation
• 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
• Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q
• Characterization of partial trisomy 9p due to insertional translocation by chromosomal (micro)FISH
• Choroid plexus hyperplasia and chromosome 9p gains
• Choroidal artery embolization in the management of cerebrospinal fluid overproduction: case report and review of the literature
• Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridization
• Clinical and molecular delineation of duplication 9p24.3q21.11 in a patient with psychotic behavior
• Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review
• Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion
• Complex chromosome re-arrangement 45,X,t(Y;9) 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
• Congenital hydrocephalus in a trisomy 9p gained child: a case report
• Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation
• 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
• De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency
• Detection of 9p partial trisomy using array-based comparative genomic hybridization
• Diagnosis of a case with partial 9p trisomy by next generation sequencing
• 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
• Exploring polycythaemia vera with fluorescence in situ hybridization: additional cryptic 9p is the most frequent abnormality detected
• Familial whole-arm translocations (1;19), (9;13), and (12;21): a review of 101 constitutional exchanges
• Gain of 9p due to an unbalanced rearrangement der(9;18): a recurrent clonal abnormality in chronic myeloproliferative disorders
• Genetic analysis of a case with a supernumerary marker derived from chromosome 9
• 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
• Good response to long-term therapy with growth hormone in a patient with 9p trisomy syndrome: A case report and review of the literature
• Hepatoblastoma in a patient with a partial trisomy 9p syndrome: a case report
• Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type
• Improved identification for trisomy 9p and partial trisomy 6q presented in a patient by array-based comparative genomic hybridization
• Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report
• Karyotype and molecular cytogenetic studies in polycythemia vera
• Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9)
• Lupus-like disease and high interferon levels corresponding to trisomy of the type I interferon cluster on chromosome 9p
• Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation (malignant triton tumor) with balanced t(7;9)(q11.2;p24) and unbalanced translocation der(16)t(1;16)(q23;q13)
• Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization
• Misdiagnosis of mosaic tetrasomy 9p in a fetus by single nucleotide polymorphism-based array
• 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 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 9p in a Patient with Mild Dysmorphic Features and Normal Intelligence
• Nail and phalangeal agenesis in a patient with 4pter and 9pter duplication
• Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation
• No Evidence of Abnormal Expression of Beta-Catenin and Bcl-2 Proteins in Pilomatricoma as One Clinical Feature of Tetrasomy 9p Syndrome
• Novel brain magnetic resonance imaging finding in a patient with trisomy 9p syndrome
• Numerical gain and structural rearrangements of JAK2, identified by FISH, characterize both JAK2617V>F-positive and -negative patients with Ph-negative MPD, myelodysplasia, and B-lymphoid neoplasms
• Oropharyngeal dysphagia and language delay in partial trisomy 9p: case report
• Partial monosomy 9p (9p22.2-->pter) and partial trisomy 18q (18q21.32-->qter) in a female infant with anorectal malformations
• Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl
• Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: an array CGH analysis and review
• Partial trisomy 3p/monosomy 9p with sex reversal
• Partial trisomy 4q and partial monosomy 9p in a girl with choanal atresia and various dysmorphic findings
• Partial trisomy 9p and 14q microduplication in a patient with growth retardation: a case report and review of the literature
• Partial trisomy 9p and partial monosomy 7p of an infant inherited from maternal balanced translocation: a case report
• Partial Trisomy 9p with Clinical Symptoms Resembling Interferonopathies
• Partial Trisomy 9p(p22→pter) from a Maternal Translocation 4q35 and 9p22
• 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 trisomy 9p and a hypoplastic left heart with a tricentric chromosome 9
• Phenotypic and cytogenetic spectrum of 9p trisomy
• Polycythemia vera transforming to acute myeloid leukemia and complex abnormalities including 9p homogeneously staining region with amplification of MLLT3, JMJD2C, JAK2, and SMARCA2
• Prenatal detection of terminal 9p24.3 microduplication encompassing DOCK8 gene: A variant of likely benign
• 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 the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion
• Prevalence and prognostic impact of allelic imbalances associated with leukemic transformation of Philadelphia chromosome-negative myeloproliferative neoplasms
• Pure 9p duplication syndrome with aplasia of the middle phalanges of the fifth fingers
• Pure 9p trisomy derived from a terminal balanced unreciprocal translocation
• Reciprocal chromosome translocations involving short arm of chromosome 9 as a risk factor of unfavorable pregnancy outcomes after meiotic malsegregation 2:2
• Self-injurious behavior associated with trisomy 9p (9p13.1 --> p24.3)
• Six cases of deletion 9p24 and trisomy 19q13.4 inherited from a familial balanced translocation
• Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter)
• Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients
• Systematic genetic analysis for a case with duplication 9p
• Tetrasomy 9q in an infant with cleft palate and multiple anomalies
• Three patients with 9p deletions including DMRT1 and DMRT2: a girl with XY complement, bilateral ovotestes, and extreme growth retardation, and two XX females with normal pubertal development
• Trisomy 9p and clinical heterogeneity: case report of an unusual presentation
• Trisomy 9p and Prader-Willi syndromes in an infant resulting from a de-novo unbalanced t(9;15) translocation
• Trisomy 9p associated with self-injured behaviour and multiple intractable keloids
• Trisomy 9p. A brief clinical, diagnostic and therapeutic description
• Trisomy 9p. Report of two new cases
• 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