Genetic counseling: Prenatal diagnosis

Submitted: Monday 26th of July 2010 06:05:58 PM
Submitted by: egf
Language: English
Educational levels: qc1, qc2, qc3

Topics

Abstract

This resource contains materials from advanced courses of genetic counseling. It is especially focused on prenatal diagnosis.

Resources

Series of lectures given in the 1st Course in Clinical Dysmorphology , hold on 9th – 12th September 2007, Bologna, Italy
This resource contains materials from advanced courses of genetic counseling. It is especially focused on prenatal diagnosis of haemoglobin disorders.
This resource contains materials from advanced courses of genetic counseling. It is especially focused on non-Invasive Prenatal Diagnosis.
This resource contains materials from advanced courses of genetic counseling. It is especially focused on new approaches in prenatal diagnosis.

Learning packages

This resource is part of the following learning package:

Similar resources


Loading ...

IMS Metadata

Keywords

abnormal, adoption, affected, affected sib-pair, agarose gel, allele, alpha, amniocentesis, amniotic fluid, Analysis of the entire coding region: Sequence analysis, anencephaly, aneuploidy, annealing, antibody, antigen, apoptosis, Array genomic hybridization, artificial insemination by donor, association, autoimmune disease, autosomal, autosomal dominant, autosomal recessive, bacterial artificial chromosome, balanced translocation, band, base, base pair, beta, biosynthesis, biotechnology, blastomere, carrier, carrier screening, cell, cell culture, centimorgan, chorion, chorionic villus sampling, chromosome, chromosome abnormality, clinical genetics, clone, codon, cohort, competent, complement, compound heterozygote, congenital, connective tissue, cordocentesis, critical region, cystic fibrosis transmembrane conductance regulator, cytogenetics, de novo, deformation, deletion, denaturing gradient gel electrophoresis, deoxyribonucleic acid, discordant, disruption, dna polymerase, domain, dominant, duplication, dysmorphic feature, dysmorphology, dysplasia, electrophoresis, embryo, exon, expression, false-negative, false-positive, familial, family history, fetus, fibroblast, fluorescent activated cell sorting, fluorescent in situ hybridization, foreign dna, frequency, gel electrophoresis, gene, gene therapy, genetic counselling, geneticist, genetics, genome, genomic dna, genotype, genotyping, growth factor, haemoglobinopathy, haplotype, haplotype analysis, helix, hereditary, hereditary persistence of fetal hb, heredity, heterozygote, heterozygous, homozygous, human leucocyte antigen, hydrocephalus, implantation, in vitro fertilisation, incomplete penetrance, index case, informative, inherited, internal control, intra-cytoplasmic sperm injection, inv, inversion, isolated, karyotype, kilobase, ligation, linkage, locus, long interspersed nuclear element, malformation, marker, maternal, maternal contamination, metabolic disorder, metabolism, metaphase, methylation, microarray, microdeletion, microsatellite, mode of inheritance, molecular genetics, monoclonal, monogenic, mutant, mutation, neonatal death, neural tube, new mutation, nucleotide, nucleus, oligonucleotide, ova, parental, penetrance, peptide, phenotype, placenta, point mutation, polar body, polymerase chain reaction, polymorphism, population, population screening, preimplantation genetic diagnosis, prenatal diagnosis, prenatal screening, primer, proband, probe, protein, qualitative, quantitative, rearrangement, recessive, reciprocal translocation, recombination, restriction enzyme, restriction fragment length polymorphism, reverse transriptase pcr, risk assessment, Robertsonian translocation, screening, segmental, selection, sensitivity, sequence, sex linked, sex-determining region of the y, sib, silent mutation, single nucleotide polymorphism, Southern blot, specificity, sperm, spina bifida, sporadic, stem cell, syndrome, synthesis, target dna, telomere, terminator, trait, transition, translocation, trisomy, trisomy rescue, ultrasound, uniparental disomy, uterus, variant, y-chromosome, zygote

Rating

0

Terms of use

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

sfy39587f01