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■ Abbreviation / Long Form : CCRs / complex chromosomal rearrangements

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Total Number of Papers: 36
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Abbreviation:   CCRs  (>> Co-occurring Abbreviation)
Long Form:   complex chromosomal rearrangements
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No. Year Title Co-occurring Abbreviation
2019 Clinical impact of chromothriptic complex chromosomal rearrangements in newly diagnosed multiple myeloma. CNV, CPL, CTH, MM
2019 Comprehensive structural variation genome map of individuals carrying complex chromosomal rearrangements. WGS
2019 Familial 3-Way Balanced Translocation Causes 1q43→qter Loss and 10q25.2→qter Gain in a Severely Affected Male Toddler. ---
2018 Clinical outcomes in carriers of complex chromosomal rearrangements: a retrospective analysis of comprehensive chromosome screening results in seven cases. PGD
2017 A de novo complex chromosome rearrangement associated with multisystematic abnormalities, a case report. AID, FISH, IVF, PGD
2017 Interstitial 10q21.1q23.31 Duplication due to Meiotic Recombination of a Paternal Balanced Complex Rearrangement: Cytogenetic and Molecular Characterization. ---
2015 Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties. ---
2014 A Rare De novo Complex Chromosomal Rearrangement (CCR) Involving Four Chromosomes in An Oligo-asthenosperm Infertile Man. AZF, CCR, FISH
2014 Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay. CMA
10  2014 The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2. MPS
11  2013 A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification. ---
12  2013 A familial Cri-du-Chat/5p deletion syndrome resulted from rare maternal complex chromosomal rearrangements (CCRs) and/or possible chromosome 5p chromothripsis. ---
13  2013 Characterization of a balanced complex chromosomal rearrangement carrier ascertained through a fetus with dup15q26.3 and del5p15.33: case report. array-CGH, three-color FISH
14  2012 Characterization of a complex rearrangement involving chromosomes 1, 4 and 8 by FISH and array-CGH. ---
15  2012 Constitutional complex chromosomal rearrangements in a klinefelter patient: case report and review of literature. ---
16  2011 Complex chromosomal rearrangements: origin and meiotic behavior. ---
17  2010 A paternally transmitted complex chromosomal rearrangement (CCR) involving chromosomes 2, 6, and 18 includes eight breakpoints and five insertional translocations (ITs) through three generations. CCR, ITs
18  2010 Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints. FISH, mBAND, SKY
19  2010 Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis. WGA
20  2009 Complex human chromosomal and genomic rearrangements. CNV, FoSTeS, MMBIR
21  2008 A complex submicroscopic chromosomal imbalance in 19p13.11 with one microduplication and two microtriplications. ---
22  2008 A healthy live birth after successful preimplantation genetic diagnosis for carriers of complex chromosome rearrangements. FISH, PGD
23  2008 Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding. MCB
24  2007 Complex chromosomal rearrangement and intracytoplasmic sperm injection: a case report. FISH, ICSI
25  2007 Complex chromosomal rearrangements. ---
26  2007 De novo complex chromosomal rearrangement of 46, XY, t (3; 16; 8) (p26; q13; q21.2) in a non-obstructive azoospermic male. ---
27  2007 Molecular cytogenetic characterization of two independent karyotypic anomalies in a patient with severe mental retardation and juvenile idiopathic arthritis. ---
28  2007 The optimization of sample treatment for spectral karyotyping with applications for human tumour cells. SKY
29  2006 Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies. ---
30  2004 Combined spectral karyotyping, multicolor banding, and microarray comparative genomic hybridization analysis provides a detailed characterization of complex structural chromosomal rearrangements associated with gene amplification in the osteosarcoma cell line MG-63. CGH, mBAND, SKY
31  2004 Fluorescence in situ hybridization characterization of apparently balanced translocation reveals cryptic complex chromosomal rearrangements with unexpected level of complexity. ---
32  2004 Molecular cytogenetic analysis of complex chromosomal rearrangements in patients with mental retardation and congenital malformations: delineation of 7q21.11 breakpoints. CGH, M-FISH
33  2003 A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected]. MR/CM
34  2003 Baseline and treatment-induced chromosomal abnormalities in peripheral blood lymphocytes of Hodgkin's lymphoma patients. CAs, HL
35  2002 Familial complex chromosomal rearrangement resulting in a recombinant chromosome. ---
36  1998 De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: report and review. CCR, FISH