• "Essentially pure" partial trisomy (6)(p23-->pter) in two brothers due to maternal t(6;17)(p23;p13.3)
• A case of de novo partial tetrasomy of distal 6p and review of the literature
• A case of partial 1p36.1 deletion and partial trisomy 6p diagnosed by karyotype
• A familial complex chromosome translocation resulting in duplication of 6p25
• Abnormalities involving chromosome 6 in newly diagnosed patients with non-Hodgkin's lymphoma. Nebraska Lymphoma Study Group
• An Adolescent with a Rare <em>De Novo</em> Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination
• An unusual case of retinopathy of prematurity
• Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion
• Brachydactyly type E in an Italian family with 6p25 trisomy
• Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomas
• Clinical expression of an inherited unbalanced translocation in chromosome 6
• Complex chromosome rearrangement of 6p25.3-&gt;p23 and 12q24.32-&gt;qter in a child with moyamoya
• Concurrent transposition of distal 6p and 20q to the 22q telomere: a recurrent benign chromosomal variant
• Craniofacial anomalies, deafness, brachydactyly, short stature, and moderate mental retardation due to a cryptic 6p;11q translocation
• Cyclin D3 immunoreactivity in follicular lymphoma is independent of the t(6;14)(p21.1;q32.3) translocation or cyclin D3 gene amplification and is correlated with histologic grade and Ki-67 labeling index
• Cyclin D3 immunoreactivity in gastrointestinal stromal tumors is independent of cyclin D3 gene amplification and is associated with nuclear p27 accumulation
• Cytotoxic and cytodifferentiative components of 6-thioguanine resistance in HL-60 cells containing acquired double minute chromosomes
• De novo "pure" partial trisomy (6)(p22.1--&gt;pter) in a chromosome 15 with an enlarged satellite, identified by microdissection
• De Novo Mosaic 6p23-p25.3 Tetrasomy Caused by a Small Supernumerary Marker Chromosome Presenting Trisomy Distal 6p Phenotype: A Case Report and Literature Review
• De-novo 'pure' partial trisomy (6)(p22.3→pter): a case report and review of the literature
• Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection
• Distal trisomy 6p and 20q owing to the concurrent transposition of distal 6p and 20q to the 22q telomere: a genomic polymorphism?
• Engraftment and growth of patient-derived retinoblastoma tumour in severe combined immunodeficiency mice
• Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: report of a new case and review of the literature
• Familial trisomy 6p in mother and daughter
• Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations
• Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia
• Glomerulopathy in patients with distal duplication of chromosome 6p
• Immunodeficiency in a child with partial trisomy 6p
• Immunoreactivity for cyclin D3 is frequently detectable in high-grade primary gastric lymphomas in the absence of the t(6;14)(p21.1;q32.3) chromosomal translocation
• Interstitial tandem duplication of 6p: a case with partial trisomy (6)(p12p21.3)
• Inversion duplication of chromosome 6 with trisomic codominant expression of HLA antigens
• IRF4 gene rearrangements define a subgroup of CD30-positive cutaneous T-cell lymphoma: a study of 54 cases
• Karyotype-phenotype correlation in partial trisomies of the short arm of chromosome 6: a family case report and review of the literature
• Mechanism of i(6p) formation in retinoblastoma tumor cells
• Molecular cytogenetic characterisation of a novel <em>de novo</em> ring chromosome 6 involving a terminal 6p deletion and terminal 6q duplication in the different arms of the same chromosome
• Molecularly defined interstitial tandem duplication 6p case with mild manifestations
• Nonrandom karyotype changes in human retinoblastomas
• Ovarian dysgenesis associated with an unbalanced X;6 translocation: first characterisation of reproductive anatomy and cytogenetic evaluation in partial trisomy 6 with breakpoints at Xq22 and 6p23
• Partial 6p trisomy associated with infantile autism
• Partial trisomy 13 as a result of de novo (6p;13q) translocation
• Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?
• Partial trisomy 6p due to maternal t(1;6) translocation
• Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues
• Partial trisomy 6p with agenesis of the corpus callosum and choanal atresia
• Paternal origin of der(X)t(X;6) in a girl with trisomy 6p and unbalanced t(6;10) mosaicism in her mother
• Perinatal diagnosis of a fetus with an unbalanced translocation 46,XY,der(10)t(6;10)(p22;q26.1) with multiple malformations:a case report and literature review
• Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry
• Prenatal diagnosis of interstitially satellited 6p
• Prognostic value of numerical chromosome aberrations in multiple myeloma: A FISH analysis of 15 different chromosomes
• Pure 6p22-pter trisomic patient: refined FISH characterization and genotype-phenotype correlation
• Pure de novo partial trisomy 6p in a girl with craniosynostosis
• Pure partial trisomy 6p due to a familial insertion (16;6)(p12;p21.2p23)
• Pure partial trisomy of 6p12.1-p22.1 secondary to a familial 12/6 insertion in two malformed babies
• Regional mapping of the HLA on the short arm of chromosome 6
• Renal complications in 6p duplication syndrome: microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS)
• Severe musculoskeletal phenotype associated with an unbalanced t(6;10) translocation: clarification of the locus for this phenotype on distal 6p
• Small supernumerary marker chromosome causing partial trisomy 6p in a child with craniosynostosis
• Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification
• Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome
• TdT positive B-cell acute lymphoblastic leukaemia (B-ALL) without Burkitt characteristics
• The spectrum of 4q- syndrome illustrated by a case series
• Trisomy 6p and ring chromosome 11 in a melanotic schwannoma suggest relation to malignant melanoma rather than conventional schwannoma
• Trisomy 6p due to a de-novo t(6;12) translocation
• Trisomy 6p in an ocular melanoma
• Trisomy of the long arm of chromosome 1 resulting in a dicentric derivative (6)t(1;6) chromosome in a child with myelodysplastic syndrome following treatment for a primitive neuroectodermal tumor
• Two familial intrachromosomal insertions with maternal dup(6)(p22.3p25.3) or dup(2)(q24.2q32.1) in recombinant offspring
• Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome
• Unbalanced 4;6 translocation and progressive renal disease
• Unbalanced translocation 6p/16q (partial monosomy 6p and trisomy 16q): prenatal diagnosis and cytogenetics
• Uterine leiomyoma cytogenetics
• Woman with UV hypersensitivity and a de novo unbalanced chromosome translocation