Chromosomal Abnormalities
Chromosomes are the structures that hold qualities. Qualities are the individual guidelines that advise our bodies how to create and work; they represent physical and therapeutic attributes, for example, hair shading, blood classification and weakness to disease.Many chromosomes have two sections, called "arms," isolated by a squeezed district known as the centromere. The shorter arm is known as the "p" arm. The more drawn out arm is known as the "q" arm.A picture, or chromosome guide, of every one of the 46 chromosomes is known as a karyotype. The karyotype can distinguish anomalies in the structure or the quantity of chromosomes.
Most chromosome irregularities happen as a mischance in the egg or sperm. In these cases, the variation from the norm is available in each cell of the body. A few irregularities, be that as it may, happen after origination; then a few cells have the variation from the norm and some do not.Chromosome anomalies can be acquired from a guardian, (for example, a translocation) or be "once more" (new to the person). This is the reason, when a kid is found to have an irregularity, chromosome studies are regularly performed on the often.
Related Conference of Chromosomal Abnormalities
18th World Congress on Advances in Stem Cell Research and Regenerative Medicine
20th World Congress on Tissue Engineering Regenerative Medicine and Stem Cell Research
18th International Conference on Human Genomics and Genomic Medicine
Chromosomal Abnormalities Conference Speakers
Recommended Sessions
- Bioprocess Engineering and Biomarkers
- Cancer Genomics
- Chromosomal Abnormalities
- Clinical applications and diagnostics
- Cytogenetics
- Ecogenomics
- Evolution of Novel Genes
- Gene Expression, Regulation And Cloning
- Gene Mapping
- Genetic counseling
- Genetic Disorders Tests
- Genetic engineering techniques
- Genetic Testing Market
- Genetically modified organisms
- Genomic analysis
- Genomic data
- Genomic medicine
- Global DNA and Gene Chip (Microarrays)
- Medical genomics
- Microbial genetics
- Molecular Medicine
- Next generation sequencing
- Novel medical Devices
- Pedigree Methods
- Personalised genomics
- Pharmacogenetics
- Polygenic inheritance
- Prenatal diagnosis
- Reprogenetics
- Teratogenesis and their effects
- Tissue culture techniques
- Tissue Engineering and Regeneration
- Transgenic Research
- Tumor Markers
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