Chromosome Aberrations Concept

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15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients Journal Articles
4.3‐Mb triplication of 4q32.1–q32.2: Report of a family through two generations Journal Articles
46,XX/46,XX,r (2)(p25q37) mosaicism: clinical and cytogenetic studies. Journal Articles
A FISH study of chromosome fusion in the ICF syndrome: involvement of paracentric heterochromatin but not of the centromeres themselves. Journal Articles
A RARE CASE OF INTERSTITIAL del(1)(p34.3p36.11) DIAGNOSED PRENATALLY Journal Articles
A UV-specific endonucleolytic activity present in human cell extracts Journal Articles
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization Journal Articles
A prenatally recognizable malformation syndrome associated with a recurrent post‐zygotic chromosome rearrangement der(Y)t(Y;1)(q12:q21) Journal Articles
ASSOCIATION BETWEEN BREUS' MOLE AND PARTIAL HYDATIDIFORM MOLE: CHANCE OR CAN HYDROPIC VILLI PRECIPITATE PLACENTAL MASSIVE SUBCHORIONIC THROMBOSIS? Journal Articles
Alterations in chromosome 1q in multiple myeloma randomized clinical trials: a systematic review Journal Articles
An inherited pericentric chromosomal inversion (46, inv3 [p-q+]) associated with skeletal anomalies Journal Articles
Analysis of IFT74as a candidate gene for chromosome 9p-linked ALS-FTD Journal Articles
Assignment by deletion of human red cell acid phosphatase gene locus to the short arm of chromosome 2. Journal Articles
Can Preference Scores for Discrete States Be Used to Derive Preference Scores for an Entire Path of Events? Journal Articles
Canadian Cytogenetic Emergency Network (CEN) for biological dosimetry following radiological/nuclear accidents Journal Articles
Cell Death Mechanisms Associated with G₂Radiosensitivity in Patients with Prostate Cancer and Benign Prostatic Hyperplasia Journal Articles
Characterization of human embryonic stem cells with features of neoplastic progression Journal Articles
Characterization of the Supernumerary Chromosome in Cat Eye Syndrome Journal Articles
Chromosomal damage induced by human adenovirus type 12 requires expression of the E1B 55-kilodalton viral protein Journal Articles
Chromosome Abnormalities in Chronic Myeloid Leukaemia Journal Articles
Chromosome investigations & clinical outcome in patients with myelodysplastic syndromes. Journal Articles
Clinical follow-up of high mid-trimester maternal serum intact human chorionic gonadotrophin concentrations in singleton pregnancies Journal Articles
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 Journal Articles
Clinically detectable copy number variations in a Canadian catchment population of schizophrenia Journal Articles
Comparative genomic hybridization detects multiple chromosomal amplifications and deletions in undifferentiated embryonal sarcoma of the liver Journal Articles
Comparison of in vivo somatic cell mutation, chromosome aberration, sister chromatid exchange, micronuclei formation and urine mutagenicity in steel foundry workers. Journal Articles
Comparison of three assays for genetic effects of antineoplastic drugs on cancer patients and their nurses Journal Articles
Cytogenetic studies: an essential part of the paediatric necropsy. Journal Articles
De novo 1q32q44 duplication and distal 1q trisomy syndrome Journal Articles
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy Journal Articles
Decision Analysis of Prenatal Testing for Chromosomal Disorders: What Do the Preferences of Pregnant Women Tell Us? Journal Articles
Definition of adenovirus type 5 functions involved in the induction of chromosomal aberrations in human cells Journal Articles
Delineation of Two Clinically and Molecularly Distinct Subgroups of Posterior Fossa Ependymoma Journal Articles
DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review. Journal Articles
Dose– and time–response relationships for lethal mutations and chromosomal instability induced by ionizing radiation in an immortalized human keratinocyte cell line Journal Articles
Down’s Syndrome Associated with a Familial (21q—;22q+) Translocation Journal Articles
ERCC1/XPF Removes the 3′ Overhang from Uncapped Telomeres and Represses Formation of Telomeric DNA-Containing Double Minute Chromosomes Journal Articles
Effects of hTERT on metal ion-induced genomic instability Journal Articles
Elevated DNA damage in a mouse model of oxidative stress: impacts of ionizing radiation and a protective dietary supplement Journal Articles
Elevated G2 chromosomal radiosensitivity in Irish breast cancer patients: a comparison with other studies Journal Articles
Expression of SV40 large T antigen, but not small t antigen, is required for the induction of chromosomal aberrations in transformed human cells Journal Articles
Expression of mutant telomerase in immortal telomerase-negative human cells results in cell cycle deregulation, nuclear and chromosomal abnormalities and rapid loss of viability Journal Articles
Fanconi's anemia: a clinico-hematological and cytogenetic study. Journal Articles
Genetic analysis of the maternal factors controlling the survival of trisomy 16 mouse fetuses Journal Articles
Genotoxicity assessment of magnetic iron oxide nanoparticles with different particle sizes and surface coatings Journal Articles
Heavy metals of relevance to human health induce genomic instability Journal Articles
Human Chromosome 7: DNA Sequence and Biology Journal Articles
Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients Journal Articles
Implication of Abnormal Human Trophoblast Karyotype for the Evidence‐Based Approach to the Understanding, Investigation, and Treatment of Recurrent Spontaneous Abortion Journal Articles
Is there any evidence for immunologically mediated or immunologically modifiable early pregnancy failure? Journal Articles
Issues in the etiology of recurrent spontaneous abortion Journal Articles
Leukemia after Chemotherapy for Cancer Journal Articles
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Journal Articles
Mechanisms and implications of genomic instability and other delayed effects of ionizing radiation exposure Journal Articles
Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7 Journal Articles
Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization. Journal Articles
Multiple congenital anomalies in a fetus with 45,X/46,X,r(X)(p11.22q12) mosaicism Journal Articles
Neonatal deaths: prospective exploration of the causes and process of end-of-life decisions Journal Articles
Nonrandom chromosomal abnormalities in bovine lymphoma Journal Articles
Particulate debris from a titanium metal prosthesis induces genomic instability in primary human fibroblast cells Journal Articles
Prenatal Diagnosis of Genetic Disorders: Trials and Tribulations Journal Articles
RETIRED: Use of Array Genomic Hybridization Technology in Prenatal Diagnosis in Canada Journal Articles
Rearrangements of chromosomal regions containing ribosomal RNA genes and centromeric heterochromatin in the human melanoma cell line MeWo Journal Articles
Relative Biological Effectiveness and Non-Poissonian Distribution of Dicentric Chromosome Aberrations following Californium-252 Neutron Exposures of Human Peripheral Blood Lymphocytes Journal Articles
Reprogramming of Telomerase by Expression of Mutant Telomerase RNA Template in Human Cells Leads to Altered Telomeres That Correlate with Reduced Cell Viability Journal Articles
Ring chromosome 22 and autism: Report and review Journal Articles
Structural Variation of Chromosomes in Autism Spectrum Disorder Journal Articles
Telomere maintenance in tumour cells. Journal Articles
The CDK inhibitor AT7519M in patients with relapsed or refractory chronic lymphocytic leukemia (CLL) and mantle cell lymphoma. A Phase II study of the Canadian Cancer Trials Group Journal Articles
The Influence of Track Structure on the Understanding of Relative Biological Effectiveness for Induction of Chromosomal Exchanges in Human Lymphocytes Journal Articles
The Lyon hypothesis Journal Articles
The hereditary adult-onset ataxias in South Africa Journal Articles
The impact of category, cytopathology and cytogenetics on development and progression of clonal and malignant myeloid transformation in inherited bone marrow failure syndromes Journal Articles
The shortest telomeres drive karyotype evolution in transformed cells Journal Articles
The usefulness of chromosome banding in pre‐ and postnatal service cytogenetics: A reconsideration Journal Articles
Therapy-Related Leukemia and Myelodysplasia in Small-cell Lung Cancer Journal Articles
Transformation of human cultured fibroblasts with plasmids carrying dominant selection markers and immortalizing potential Journal Articles
Tumorigenicity of ten karyotypically distinct cell types present in the human melanoma cell line MeWo-A Journal Articles
Two Cases of Fibrocystic Breast Disease with Polysomy 18 as the Sole Clonal Cytogenetic Abnormality Journal Articles
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder Journal Articles
Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation Journal Articles
‘Putting our heads together’: insights into genomic conservation between human and canine intracranial tumors Journal Articles
“High-grade oncocytic renal tumor”: morphologic, immunohistochemical, and molecular genetic study of 14 cases Journal Articles