Molecular Cytogenetics

Submitted: Wednesday 4th of August 2010 06:04:00 PM
Submitted by: egf
Language: English
Educational levels: expert, qc1, qc2, qc3



This resource contains materials from advanced courses of cytogenetics and it is especially focused on Molecular Cytogenetics


This resource contains materials from advanced courses of cytogenetics and it is especially focused on Molecular Cytogenetics.
This resource contains materials from advanced courses of cytogenetics and it is especially focused on DNA Copy Number Variations Analysis.
This resource contains materials from advanced courses of cytogenetics and it is especially focused on Fluorescence In Situ Hybridization (FISH).
This resource contains materials from advanced courses of cytogenetics and it is especially focused on Comparative Genomic Hybridisation (CGH).
This resource contains materials from advanced courses of cytogenetics and it is especially focused on next generation approaches.

Learning packages

This resource is part of the following learning package:

Similar resources

Loading ...

IMS Metadata


18s ribosomal rna, 5s ribosomal rna, abnormal, acentric, acetylation, acrocentric, adenosine triphosphate, affected, agarose gel, algorithm, allele, allele frequency, alpha, alu-pcr, amino acid, amniocentesis, amniotic fluid, Analysis of the entire coding region: Mutation scanning, Analysis of the entire coding region: Sequence analysis, anaphase lag, ancestral haplotype, aneuploidy, annealing, antibody, antigen, antigen binding fragment, antisense oligonucleotide, apolipoprotein, apoptosis, Array genomic hybridization, artificial insemination by donor, ascertainment, association, association studies, autism, autosomal, autosomal dominant, autosomal recessive, autosome, b lymphocytes, bacterial artificial chromosome, balanced translocation, band, banding, base, base pair, benign variant, beta, bias of ascertainment, bioinformatics, biomarker, biotechnology, bivalent, blastomere, BRCA, break-point cluster, cancer genetics, candidate gene, carrier, carrier testing, cell, cell culture, cell cycle, cell line, centimorgan, centromere, chi-square, chiasma, chorion, chorionic villus sampling, chromatin, chromosomal analysis, chromosome, chromosome abnormality, chromosome painting, chromosome translocation, chromosome walking, cis configuration, clinical geneticist, clinical genetics, clone, cloning, coding region, coding sequence, cohort, common disease, comparative genomics, complement, Complementary DNA, complementary strand, conception, concordance, congenital, consanguinity, constitutional, contigs, contiguous gene syndrome, control gene, copy number polymorphism, correlation, cosmid, coupling, cpg island, critical region, Cytogenetic Abnormality, Cytogenetic Analysis, cytogenetics, cytoplasm, cytosol, de novo, degenerate oligonucleotide-primed pcr, deletion, Deletion-duplication analysis, deoxyribonucleic acid, derivative chromosome, diagnostic testing, diakinesis, diallelic, differentiate, diploid, disjunction, disruption, dna haplotype, dna library, dna microarray, dna polymerase, dna probe, dna structure, domain, dominant, drift, duplication, dynamic mutation, dysmorphic feature, dysmorphology, dysplasia, dystrophin, electrophoresis, embryo, embryonic stem cell, enhancer, enzyme, epigenetics, ER, euchromatin, exon, expansion, expectation maximization algorithm, expressed gene, expression, familial, fetus, fibroblast, FISH-interphase, FISH-metaphase, fixed, flow cytometry, flow karyotype, Fluorescence in situ Hybridization, fluorescent activated cell sorting, fluorescent dye, fluorescent in situ hybridization, founder, fragile site, frameshift mutation, framework map, frequency, g band, gametogenesis, gene, gene amplification, gene cloning, gene conversion, gene expression, gene targeting, gene therapy, genetic counselling, genetic disease, genetic map, genetic mapping, genetic marker, genetic variation, genetics, genome, genome wide association, genomic dna, genomics, genotype, genotyping, germ cell, germline, gm, gray, growth factor, haploid, haplotype, hapmap project, helicase, helix, hemizygous, hereditary, heredity, heterochromatin, heterogeneity, heteromorphism, heterozygote, heterozygous, high throughput, homogeneously staining region, homologous, homologous chromosome, homologous recombination, homozygote, homozygous, hormone, hotspot, housekeeping gene, human genome project, Human immunodeficiency virus, human leucocyte antigen, huntingtin, hybrid, hybridization, hydatidiform mole, immune system, immunoglobulin, immunohistochemistry, implantation, in situ hybridization, in vitro, in vivo, incidence, incomplete penetrance, index case, informative, informed consent, inherited, innate immunity, insertion, internal control, interphase, interphase cytogenetics, interstitial deletion, intron, inv, inversion, isochromosome, isolate, isolated, karyogram, karyotype, kilobase, leucine zipper, library, ligase, ligation, linkage, linkage disequilibrium, locus, locus control region, long interspersed nuclear element, long terminal repeat, loss of heterozygosity, malformation, marker, marker chromosome, maternal, megabase, meiosis, meiotic prophase I, mendelian inheritance, messenger rna, metabolism, metaphase, metastasis, methylation, methylation analysis, microarray, microdeletion, microdeletion syndrome, microrna, microsatellite, microtubules, minor allele frequency, miscarriage, mismatch repair mechanism, missense mutation, mitochondrial dna, mitosis, Molecular Analysis, molecular genetics, monogenic, monosomy, monozygotic twins, mosaic, mosaicism, multiallelic, Multicolor FISH, multiple alleles, multivariate, mutant, mutation, mutation rate, myeloma, new mutation, nondisjunction, nonsense mutation, northern blot, nucleotide, nucleus, oligonucleotide, oncogene, oncogenic, open reading frame, orthologous, p1-derived artificial chromosome, pachytene, paint, paracentric inversion, paralogous, parental, pedigree, penetrance, peptide, pericentric, pericentric inversion, pharmacogenetics, phase, phenotype, phenotypic variation, physical map, placenta, plasmid, point mutation, polymerase, polymerase chain reaction, polymorphic marker, polymorphism, population, posterior probability, power, predisposition, preimplantation diagnosis, preimplantation genetic diagnosis, prenatal diagnosis, prenatal screening, prevalence, primer, probability, proband, probe, processing, promoter, propagation, prophase, prostate, protein, proteome, proto-oncogene, pseudoautosomal, pseudogene, quantitative, quantitative PCR, radiation absorbed dose, radiation hybrid, real-time pcr, rearrangement, recessive, reciprocal translocation, recombinant, recombination, regression, repeat unit, repetitive dna, replication, response element, restriction enzyme, restriction site, reverse transcriptase, reverse transriptase pcr, ribonucleic acid, ribosomal RNA, ring chromosome, rna interference, Robertsonian translocation, satellite, satellite dna, screening, segmental, segmental duplication, segregation, segregation analysis, selection, sensitivity, sequence, sex chromosome, sex-determining region of the y, short interspersed nuclear elements, sib, signal transduction, simple repeat, single nucleotide polymorphism, somatic, somatic cell hybrid, somatic mosaicism, somatic mutation, Southern blot, specie, specificity, Spectral Karyotyping, sperm, spina bifida, spindle, splice site, splicing, spontaneous abortion, sporadic, stem cell, substitution, subtelomeric region, survival, switching, synapsis, synaptonemal complex, syndrome, synthesis, t lymphocyte, t-cell, tagging snp, tandem repeat, target dna, telomere, tetrasomy, threshold, trait, trans-acting, transcript, transcription, transcription factor, transformation, transition, translation, translocation, trisomy, trisomy rescue, tumor suppressor gene, ultrasound, unaffected, unbalanced translocation, uniparental disomy, untranslated region, variable expressivity, variance, variant, variation, vector, virus, x-chromosome, y-chromosome, yeast artificial chromosome, zinc finger



Terms of use

This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License. Read more.