Chromosome Aberrations
Concept
Vocabulary Service
Overview
subject area of
-
15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients Academic Article
-
4.3-Mb triplication of 4q32.1-q32.2: Report of a family through two generations Academic Article
-
46,XX/46,XX,r (2)(p25q37) mosaicism: clinical and cytogenetic studies. Academic Article
-
A RARE CASE OF INTERSTITIAL del(1)(p34.3p36.11) DIAGNOSED PRENATALLY Academic Article
-
A UV-specific endonucleolytic activity present in human cell extracts Academic Article
-
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization Academic Article
-
A prenatally recognizable malformation syndrome associated with a recurrent post-zygotic chromosome rearrangement der(Y)t(Y;1)(q12:q21) Academic Article
-
ASSOCIATION BETWEEN BREUS' MOLE AND PARTIAL HYDATIDIFORM MOLE: CHANCE OR CAN HYDROPIC VILLI PRECIPITATE PLACENTAL MASSIVE SUBCHORIONIC THROMBOSIS? Academic Article
-
An inherited pericentric chromosomal inversion (46, inv3 [p-q+]) associated with skeletal anomalies Academic Article
-
Analysis of IFT74as a candidate gene for chromosome 9p-linked ALS-FTD Academic Article
-
Can Preference Scores for Discrete States Be Used to Derive Preference Scores for an Entire Path of Events? Academic Article
-
Canadian Cytogenetic Emergency Network (CEN) for biological dosimetry following radiological/nuclear accidents Academic Article
-
Cell Death Mechanisms Associated with G2Radiosensitivity in Patients with Prostate Cancer and Benign Prostatic Hyperplasia Academic Article
-
Cell cycle and clinical characteristics of patients with acute myeloid leukemia and myelodysplasia whose biopsies are reactive with anti-factor VIII antibody Academic Article
-
Characterization of human embryonic stem cells with features of neoplastic progression Academic Article
-
Characterization of the Supernumerary Chromosome in Cat Eye Syndrome Academic Article
-
Chromosomal damage induced by human adenovirus type 12 requires expression of the E1B 55-kilodalton viral protein Academic Article
-
Chromosome Abnormalities in Chronic Myeloid Leukaemia Academic Article
-
Chromosome investigations & clinical outcome in patients with myelodysplastic syndromes. Academic Article
-
Chromosome studies at the paediatric necropsy Academic Article
-
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 Academic Article
-
Clinically detectable copy number variations in a Canadian catchment population of schizophrenia Academic Article
-
Comparative genomic hybridization detects multiple chromosomal amplifications and deletions in undifferentiated embryonal sarcoma of the liver Academic Article
-
Cytogenetic studies: an essential part of the paediatric necropsy. Academic Article
-
Cytogenetic survey of a hospital for the mentally retarded Academic Article
-
De novo 1q32q44 duplication and distal 1q trisomy syndrome Academic Article
-
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy Academic Article
-
Decision Analysis of Prenatal Testing for Chromosomal Disorders: What Do the Preferences of Pregnant Women Tell Us? Academic Article
-
Definition of adenovirus type 5 functions involved in the induction of chromosomal aberrations in human cells Academic Article
-
Delineation of Two Clinically and Molecularly Distinct Subgroups of Posterior Fossa Ependymoma Academic Article
-
DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review. Academic Article
-
Dose– and time–response relationships for lethal mutations and chromosomal instability induced by ionizing radiation in an immortalized human keratinocyte cell line Academic Article
-
Down’s Syndrome Associated with a Familial (21q—;22q+) Translocation Academic Article
-
ERCC1/XPF Removes the 3′ Overhang from Uncapped Telomeres and Represses Formation of Telomeric DNA-Containing Double Minute Chromosomes Academic Article
-
Effects of hTERT on metal ion-induced genomic instability Academic Article
-
Elevated DNA damage in a mouse model of oxidative stress: impacts of ionizing radiation and a protective dietary supplement Academic Article
-
Elevated G2 chromosomal radiosensitivity in Irish breast cancer patients: a comparison with other studies Academic Article
-
Expression of SV40 large T antigen, but not small t antigen, is required for the induction of chromosomal aberrations in transformed human cells Academic Article
-
Expression of mutant telomerase in immortal telomerase-negative human cells results in cell cycle deregulation, nuclear and chromosomal abnormalities and rapid loss of viability Academic Article
-
Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers Academic Article
-
Fanconi's anemia: a clinico-hematological and cytogenetic study. Academic Article
-
Genetic analysis of the maternal factors controlling the survival of trisomy 16 mouse fetuses Academic Article
-
Genetic aspects of female reproduction Academic Article
-
Heavy metals of relevance to human health induce genomic instability Academic Article
-
High-Accuracy Relative Biological Effectiveness Values Following Low-Dose Thermal Neutron Exposures Support Bimodal Quality Factor Response with Neutron Energy Academic Article
-
Human Chromosome 7: DNA Sequence and Biology Academic Article
-
Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients Academic Article
-
Implication of Abnormal Human Trophoblast Karyotype for the Evidence-Based Approach to the Understanding, Investigation, and Treatment of Recurrent Spontaneous Abortion Academic Article
-
Is there any evidence for immunologically mediated or immunologically modifiable early pregnancy failure? Academic Article
-
Issues in the etiology of recurrent spontaneous abortion Academic Article
-
Leukemia after Chemotherapy for Cancer Academic Article
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Academic Article
-
Mechanisms and implications of genomic instability and other delayed effects of ionizing radiation exposure Academic Article
-
Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization. Academic Article
-
Multiple congenital anomalies in a fetus with 45,X/46,X,r(X)(p11.22q12) mosaicism Academic Article
-
Neonatal deaths: prospective exploration of the causes and process of end-of-life decisions Academic Article
-
Nonrandom chromosomal abnormalities in bovine lymphoma Academic Article
-
Particulate debris from a titanium metal prosthesis induces genomic instability in primary human fibroblast cells Academic Article
-
Prenatal Diagnosis of Genetic Disorders: Trials and Tribulations Academic Article
-
RETIRED: Use of Array Genomic Hybridization Technology in Prenatal Diagnosis in Canada Academic Article
-
Rearrangements of chromosomal regions containing ribosomal RNA genes and centromeric heterochromatin in the human melanoma cell line MeWo Academic Article
-
Relative Biological Effectiveness and Non-Poissonian Distribution of Dicentric Chromosome Aberrations following Californium-252 Neutron Exposures of Human Peripheral Blood Lymphocytes Academic Article
-
Reprogramming of telomerase by expression of mutant telomerase RNA template in human cells leads to altered telomeres that correlate with reduced cell viability Academic Article
-
Ring chromosome 22 and autism: Report and review Academic Article
-
Structural Variation of Chromosomes in Autism Spectrum Disorder Academic Article
-
Telomere maintenance in tumour cells. Academic Article
-
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 Academic Article
-
The Influence of Track Structure on the Understanding of Relative Biological Effectiveness for Induction of Chromosomal Exchanges in Human Lymphocytes Academic Article
-
The Lyon hypothesis Academic Article
-
The impact of category, cytopathology and cytogenetics on development and progression of clonal and malignant myeloid transformation in inherited bone marrow failure syndromes Academic Article
-
The shortest telomeres drive karyotype evolution in transformed cells Academic Article
-
The usefulness of chromosome banding in pre- and postnatal service cytogenetics: A reconsideration Academic Article
-
Therapy of Secondary Acute Nonlymphocytic Leukemia with Cytarabine Academic Article
-
Transformation of human cultured fibroblasts with plasmids carrying dominant selection markers and immortalizing potential Academic Article
-
Tumorigenicity of ten karyotypically distinct cell types present in the human melanoma cell line MeWo-A Academic Article
-
Two Cases of Fibrocystic Breast Disease with Polysomy 18 as the Sole Clonal Cytogenetic Abnormality Academic Article
-
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder Academic Article
-
“High-grade oncocytic renal tumor”: morphologic, immunohistochemical, and molecular genetic study of 14 cases Academic Article