• 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization
• A case of distal 9q trisomy syndrome associated with an unusual inheritance of ABO blood type
• A case of partial trisomy 9pter --> q13 due to paternal balanced translocation t (9;21) (q13;q21)
• A cryptic unbalanced translocation t(2;9)(p25.2;q34.3) causes the phenotype of 9q subtelomeric deletion syndrome and additional exophthalmos and joint contractures
• A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
• A malformed girl with duplication of chromosome 9q
• A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33
• Abnormalities of chromosomes 1p34-36, 4p16, 4q35, 9q11-32 and +7 represent novel recurrent cytogenetic rearrangements in chronic lymphocytic leukemia
• Adult case of partial trisomy 9q
• 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
• Brief report. Adult patient presenting an interstitial (9) (q21.32q31.1) direct duplication resulting from the malsegregation of a paternal balanced insertional translocation
• Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q
• Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review
• Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype
• Common cytogenetic findings in gastric cancer
• Concomitant presence of trisomy 21 and del(9q) in acute myeloid leukemia
• Constitutional mosaicism for a chromosome 9 inversion resulting in recombinant aneusomy in an offspring
• Cytogenetic findings in chronic myelogenous leukemia
• Cytogenetic investigation of transitional cell carcinomas of the upper urinary tract
• De novo 9q gain in an infant with tetralogy of Fallot with absent pulmonary valve: Patient report and review of congenital heart disease in 9q duplication syndrome
• Double partial trisomy 9q34.1-->qter and 21pter-->q22.11: FISH and clinical findings
• Duplication 9p and their implication to phenotype
• Duplication of 9q12-q33: a case report and implications for the dup(9q) syndrome
• Duplication of Ph and of 9q+ chromosomes during the blastic transformation of a CML case
• Familial 9q22.3 microduplication spanning PTCH1 causes short stature syndrome with mild intellectual disability and dysmorphic features
• Fusion of 9 beta-satellite and telomere (TTAGGG)n sequences results in a jumping translocation
• Gain of 9p in the pathogenesis of polycythemia vera
• High incidence of trisomies 1q, 9q, and 11q in multiple myeloma: results from a comprehensive molecular cytogenetic analysis
• Insulin-like growth factor serum concentrations reflect insufficient growth in a hypoplastic infant with partial trisomy 9q in the 12th week of life
• Interstitial 9q deletion in T-lymphoid/myeloid biphenotypic leukaemia
• Interstitial deletion of 9q revisited
• Inversion-duplication of bands q13----q21 of human chromosome 9
• Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p)
• Masked Philadelphia chromosome due to atypical BCR/ABL localization on the 9q34 band and duplication of the der(9) in a case of chronic myelogenous leukemia
• Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review
• Molecular cytogenetic studies of duplication 9q32-->q34.3 inserted into 9q13
• Monosomy 9q and trisomy 16q in a case of congenital solitary infantile myofibromatosis
• Oligodontia in partial trisomy 9q syndrome
• Partial and complete trisomy 9: delineation of a trisomy 9 syndrome
• Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26)
• Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report
• Partial trisomy 9q due to maternal 9q 17q translocation
• Partial trisomy 9q syndrome with a de novo tandem duplication of 9q22.2-q31.1
• Partial trisomy 9q: description of a new case
• Patient with partial trisomy 9q and learning disability but no pyloric stenosis
• Patient with trisomy 9p and a hypoplastic left heart with a tricentric chromosome 9
• Phenotype resembling Donnai-Barrow syndrome in a patient with 9qter;16qter unbalanced translocation
• Phenotype-genotype correlation of a patient with a "balanced" translocation 9;15 and cryptic 9q34 duplication and 15q21q25 deletion
• Phenotypical manifestations of partial trisomy 9 and monosomy 4 in two siblings
• Secondary acute myelogenous leukemia (AML) with trisomy 10 and del(9q) following precursor B-cell acute lymphoblastic leukemia (ALL) with a hyperdiploid karyotype
• Submicroscopic deletion 9(q34.3) and duplication 19(p13.3): identified by subtelomere specific FISH probes
• t(9/22) with centric fission and NOR translocation leading to a case of pure 9p trisomy in the offspring
• Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy
• Tetrasomy 9q in an infant with cleft palate and multiple anomalies
• Three cases of partial trisomy 9q in one generation due to maternal reciprocal t(6;8;9) translocation
• Trisomy 9q3 syndrome: a case report and review of the literature
• Trisomy of chromosome 9q: specific chromosome change associated with tumorigenicity during the process of X-ray-induced neoplastic transformation in golden hamster embryo cells
• Unbalanced cryptic translocation der(14)t(9;14)(q34.3;q32.33) identified by subtelomeric FISH
• Unbalanced subtelomic rearrangement involving 9q and 22q in a child with mental retardation and multiple congenital anomalies