• "Essentially" pure trisomy 3q27 --> qter: further delineation of the partial trisomy 3q phenotype
• 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 boy with partial trisomy of chromosome 3q24-q28 from paternal balanced insertion and multiple congenital anomalies
• A girl with inverted triplication of chromosome 3q25.3 --> q29 and multiple congenital anomalies consistent with 3q duplication syndrome
• A large kindred with an INV(3)(p25q23): clinical, cytogenetic and genetic marker studies
• A marginal zone phenotype in follicular lymphoma with t(14;18) is associated with secondary cytogenetic aberrations typical of marginal zone lymphoma
• A novel case of unilateral blepharophimosis syndrome and mental retardation associated with de novo trisomy for chromosome 3q
• A novel unbalanced whole-arm translocation der(3;10)(q10;q10) in acute monocytic leukemia
• A rare chromosomal disorder in a newborn: Trisomy 3q
• A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion
• Acute eosinophilic leukemia in a patient with preexistent myelodysplastic syndrome
• Analysis of 3p allelic loss in papillary and nonpapillary renal cell carcinomas. Correlation with tumor karyotypes
• Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs
• Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes
• Chromosome abnormalities in myelofibrosis
• Clear-cell and papillary carcinoma of the kidney: an analysis of chromosome 3, 7, and 17 abnormalities by microsatellite amplification, cytogenetics, and fluorescence in situ hybridization
• Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factor
• Coexistence of neocentromeric marker 3q and trisomy 3 in two different tissues in a 3-year-old boy with peripheral T-cell lymphoma: support for a gene dosage effect hypothesis
• Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32-q27.2
• Concomitant partial tetrasomy 3q and trisomy 18 in Waldenström macroglobulinemia
• Concomitant tetrasomy 3q and trisomy 18 in CD5(-), CD13(+) chronic lymphocytic leukemia
• Cytogenetic and molecular delineation of a region of chromosome 3q commonly gained in marginal zone B-cell lymphoma
• Cytogenetic profile of Indian patients with de novo myelodysplastic syndromes
• Cytogenetic study of 11 gastric adenocarcinomas
• Derivative (22)t(3;22)(q12;p11.1) in desmoplastic medulloblastoma
• Dicentric chromosome 3 associated with binucleated lymphocytes in atypical B-cell chronic lymphoproliferative disorder
• Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data
• Distal trisomy 3q as a risk factor for neural tube defects
• Duplication 3q syndrome: molecular delineation of the critical region
• Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9
• Evolution of tumor chromosome abnormalities after therapy in a pediatric astrocytoma
• Familial complex 3q;10q rearrangement unraveled by subtelomeric FISH analysis
• Familial partial trisomy of the long arm of chromosome 3 (3q)
• Familial transmission of a 3q;22p translocation, with partial trisomy of chromosome 3 in the propositus
• First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterization
• Gain of chromosome 3/3q in B-cell chronic lymphoproliferative disorder is associated with plasmacytoid differentiation with or without IgM overproduction
• Genetic analysis of splenic lymphoma with villous lymphocytes: a Groupe Français d'Hématologie Cellulaire (GFHC) study
• Genetic analysis of tumorigenesis: XVI. Chromosome changes in azacytidine- and insulin-induced tumorigenesis
• Genomic abnormalities acquired in the blastic transformation of splenic marginal zone B-cell lymphoma
• Histology may depend on the presence of partial monosomy or partial trisomy 3 in renal cell carcinoma
• Inconsistency of omphalocoele contents in three consecutive siblings with partial trisomy 3q and partial monosomy 11q
• Inherited unbalanced reciprocal translocation with 3q duplication and 5p deletion in a foetus revealed by cell-free foetal DNA (cffDNA) testing: a case report
• Mild Phenotype of Xq Deletion and 3q Duplication Associated with der(X)t(X;3)(q21.1;q22.1) without Loss of XIST Gene
• Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy
• Molecular genetics and diagnosis of renal cell tumors
• Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy
• Mosaicism for trisomy 3q arising from an unbalanced, de novo t(3;15)
• Multiple congenital malformations including severe eye anomalies and abnormal cerebellar development with Dandy-Walker malformation in a girl with partial trisomy 3q
• Multiple hemangiomas in a patient with a t(3q;4p) translocation: an infrequent association with Wolf-Hirschhorn syndrome
• Multipoint interphase FISH analysis of chromosome 3 abnormalities in 28 childhood AML patients
• Multipoint interphase FISH in childhood T-acute lymphoblastic leukemia detects subpopulations that carry different chromosome 3 aberrations
• New chromosomal dysmorphic syndromes. 3. Partial trisomy 3q
• New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception
• Non-random chromosome rearrangements in herpes simplex virus type 1 transformed diploid CHEF cells
• Nonrandom chromosomal alterations in nickel-transformed Chinese hamster embryo cells
• Numerical chromosomal changes and risk of development of myelodysplastic syndrome--acute myeloid leukemia in patients with Fanconi anemia
• Ocular findings in partial trisomy 3q. A case report and review of the literature
• Omphalocele in trisomy 3q: further delineation of phenotype
• Papillary renal cell carcinoma with clear cell cytomorphology and chromosomal loss of 3p
• Partial 3q duplication syndrome and assignment of D3S5 to 3q25-3q28
• Partial 3q-trisomy (q22-qter) monosomy 13q (q32-qter) by translocation between paternal chromosome 3 and 13
• Partial deletion of the short arm of chromosome 3. Report of a case (author's transl)
• Partial duplication of 3q and distal deletion of 10q inherited from a maternal balanced translocation
• Partial trisomy 19p: case report and natural history
• Partial trisomy 3q and the mild Cornelia de Lange syndrome phenotype
• Partial trisomy 3q causing mild Cornelia de Lange phenotype
• Partial trisomy 3q in a child with sacrococcygeal teratoma and Cornelia de Lange syndrome phenotype
• Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1; p23)
• Partial trisomy 3q. Contribution of a new case to the literature
• Partial trisomy of 3q detected by chromosome painting in a case of juvenile chronic myelomonocytic leukemia
• Partial trisomy of chromosome 3 (3q12 leads to qter) owing to 3q/18p translocation. A trisomy 3q syndrome
• PRENATAL DIAGNOSIS OF FOETAL TRISOMY 3Q WITH PATERNAL ORIGIN
• Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints
• Prenatal diagnosis of partial trisomy 3q in a fetus
• Prenatal diagnosis of partial trisomy 3q resulting from t(3;14) in a fetus with multiple anomalies including vermian hypoplasia
• Prenatal diagnosis of partial trisomy 3q(3q22-->qter) and monosomy 6q(6q25.3-->qter) in a fetus with sonographic findings of cystic hygromata colli and unilateral pleural effusion
• Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement
• Prenatal identification of partial 3q duplication syndrome
• Prenatally diagnosed partial trisomy 3q case with an omphalocele and less severe phenotype
• Probing the human genome in search for a new 3q syndrome
• Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement
• Recurrent omphalocele with partial trisomy 3q and partial monosomy 11q
• Retrospective evaluation of the clinical and laboratory data from 300 patients of various hematological malignancies with chromosome 3 abnormalities
• Specific subtelomere loss on chromosome der(11)t(3;11)(q23;q23)x2 in anaplastic thyroid cancer cell line OCUT-1
• Subchromosomal band interval mapping and ordering of DNA markers in the region 3q26.3-q27 involved in the dup(3q) syndrome
• Trisomy 17 in a bonobo (Pan paniscus) and deletion of 3q in a lowland gorilla (Gorilla gorilla gorilla): comparison with human trisomy 18 and human deletion 4q syndrome
• Trisomy 3q : two clinically similar but cytogenetically different cases
• Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype
• Trisomy for the distal part of the short arm of the number 3 chromosome in 3 siblings. First example of chromosomal insertion: INS(7;3)(q 31;p 21 p 26)
• Unbalanced t(3;12) in a case of juvenile myelomonocytic leukemia (JMML) results in partial trisomy of 3q as defined by FISH
• Unbalanced translocation (3;5)(q26.1;p14): a clinical report