Clinical Cytogenetics

Submitted: Wednesday 4th of August 2010 05:28:20 PM
Submitted by: egf
Language: English
Educational levels: expert, qc1, qc2, qc3

Topics

Abstract

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

Resources

This resource contains materials from advanced courses of cytogenetics and it is especially focused on Clinical Cytogenetics
This resource contains materials from advanced courses of cytogenetics and it is especially focused on Cancer Cytogenetics.
This resource contains materials from advanced courses of cytogenetics and it is especially focused on Pre-natal and post-natal diagnosis in clinical cytogenetics.
This resource contains materials from advanced courses of cytogenetics and it is especially focused on Genomic Disorders of Chromosome 22.

Learning packages

This resource is part of the following learning package:

Similar resources


Loading ...

IMS Metadata

Keywords

abnormal, acentric, Acquired immunodeficiency syndrome, adenomatous polyposis coli, affected, allele, alpha, alternative splicing, Analysis of the entire coding region: Mutation scanning, Analysis of the entire coding region: Sequence analysis, aneuploidy, antibody, antigen, antigen binding fragment, apoptosis, Array genomic hybridization, association, association studies, autism, autoimmune disease, autosomal, autosomal dominant, autosomal recessive, autosome, azoospermia, bacterial artificial chromosome, balanced translocation, band, banding, base, base pair, beta, bioinformatics, biomarker, break-point cluster, candidate gene, carrier, cell, cell division, cell line, centromere, chiasma, chorionic villus sampling, chromatin, chromosome, chromosome abnormality, chromosome walking, cis configuration, clone, cloning, coding region, coding sequence, common disease, Complementary DNA, confined placental mosaicism, congenital, conjugation, connective tissue, constitutional, contiguous gene syndrome, copy number polymorphism, correlation, cosmid, critical region, Cytogenetic Abnormality, Cytogenetic Analysis, cytogenetics, de novo, deletion, deoxyribonucleic acid, derivative chromosome, diagnostic test, dicentric, differentiate, diploid, discordant, disomy, dispermy, disruption, DNA methylation, dna microarray, dna polymorphisms, dna probe, dna replication, dna sequencing, domain, duplication, dysmorphic feature, dysplasia, egg, embryo, enhancer, environmental factor, enzyme, euchromatin, exon, expectation maximization algorithm, expressed gene, expression, familial, familial adenomatous polyposis, fertilisation, fetus, fibroblast, FISH-metaphase, fitness, fixed, flow karyotype, fluorescent activated cell sorting, fluorescent in situ hybridization, founder effect, frameshift, frequency, gain-of-function, gamete, gametogenesis, gene, gene amplification, gene chip, gene cloning, gene expression, gene locus, gene regulation, genetic counselling, genetic marker, genetic variation, genetics, genome, genome wide association, genomic dna, genomic imprinting, genomics, genotype, germ cell, glycoprotein, haploinsufficiency, haplotype, hemizygous, heredity, hermaphrodite, heterochromatin, heterogeneous, heteromorphism, heterozygous, high throughput, histone, homeobox, homogeneity, homogeneously staining region, homologous, homologous chromosome, homologous recombination, homozygous, hormone, hotspot, human genome project, Human immunodeficiency virus, hybrid, hybridization, immunohistochemistry, implantation, imprinting, in vitro, incidence, indels, index case, informative, inheritance, inherited, insertion, interphase, interstitial deletion, intron, inv, inversion, isochromosome, isolated, karyotype, kilobase, library, ligation, linkage, linkage analysis, linkage disequilibrium, locus, locus control region, loss of heterozygosity, malformation, marker, marker chromosome, maternal, meiosis, messenger rna, metabolism, metaphase, methylation, microarray, microdeletion, microdeletion syndrome, microrna, microsatellite, miscarriage, mitosis, modifier gene, monosomy, mosaic, mosaicism, Multicolor FISH, multifactorial, multivariate, mutant, mutation, natural selection, non-disjunction, nondisjunction, nonsense mutation, nucleotide, nullisomy, oligonucleotide, oncogene, oncogenic, pachytene, paracentric inversion, parental, penetrance, phenotype, plasmid, point mutation, polymerase chain reaction, polymorphism, population, power, predisposition, prenatal diagnosis, primer, probability, proband, probe, processing, promoter, prophase, prostate, protein, proto-oncogene, pseudoautosomal, pseudogene, quantitative, rearrangement, recessive, recessive allele, recessive gene, reciprocal translocation, recombination, regression, replication, repressor, reverse transriptase pcr, ribonucleic acid, ring chromosome, Robertsonian translocation, s phase of the cell cycle, satellite, screening, segmental, segmental duplication, segregation, selection, sensitivity, sequence, sex chromosome, sex-determining region of the y, sib, signal transduction, silencer, single nucleotide polymorphism, sister chromatids, somatic cell, somatic cell hybrid, somatic mosaicism, specie, specificity, Spectral Karyotyping, sperm, splicing, spontaneous abortion, sporadic, substitution, subtelomeric region, survival, switching, synapsis, synaptonemal complex, syndrome, synthesis, target dna, telomere, trait, transcript, transcription factor, transformation, transgenic, translocation, trisomy, tumor suppressor gene, unaffected, unbalanced translocation, unequal crossing over, uninformative, uniparental disomy, uniparental disomy study, uniparental heterodisomy, uniparental isodisomy, untranslated region, uterus, variant, variation, vector, virus, x-chromosome, x-inactivation, y-chromosome, yeast artificial chromosome

Rating

0

Terms of use

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

sfy39587f01