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retinitis pigmentosa - Foundation Fighting Blindness
retinitis pigmentosa - Foundation Fighting Blindness

... discriminate colors and perceive details. RP is typically diagnosed in adolescents and young adults. It is a progressive disorder. The rate of progression and degree of visual loss varies from person to person. Most people with RP are legally blind by age 40, with a central visual field of less than ...
Prenatal Testing for Genetic Disorders
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... Prenatal Testing for Genetic Disorders  Prenatal testing tests a fetus for genetic disorders (e.g. cystic fibrosis, Tay Sacs, ) or chromosome abnormalities (e.g. Down syndrome) In most cases, testing is done only when there is a family history or some other indication, like advanced maternal age, ...
Direct-to-Consumer Genetic Testing
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... Direct-to-consumer (DTC) genetic testing is over-the-counter genetic testing available online to consumers through private companies Generally, results report an individual’s probabilistic risk to develop a medical condition based on genome wide association studies (GWAS) Interpret DTC results with ...
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... cells). Eukaryotic multicellular organisms reproduce sexually by combining two gametes containing homologous chromosomes (one set of chromosomes from each parent) during fertilization. Crossing over during meiosis allows for the reshuffling of genetic combinations between individual homologous chrom ...
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Why are recessive disorders more common than dominant ones?

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Genetic Testing for Endocrine Gland Cancer Susceptibility

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... Lesson Objectives We are learning:  That genetic information is found in the nucleus of every cell in the body and determines characteristics.  That genetic information is inherited from parents and that in each pair of chromosomes one is inherited from the mother and one from the father.  That ...
Genetic and Molecular Diagnostic Testing
Genetic and Molecular Diagnostic Testing

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Genetic testing

Genetic testing, also known as DNA testing, allows the genetic diagnosis of vulnerabilities to inherited diseases, and can also be used to determine a child's parentage (genetic mother and father) or in general a person's ancestry or biological relationship between people. In addition to studying chromosomes to the level of individual genes, genetic testing in a broader sense includes biochemical tests for the possible presence of genetic diseases, or mutant forms of genes associated with increased risk of developing genetic disorders.Genetic testing identifies changes in chromosomes, genes, or proteins. The variety of genetic tests has expanded throughout the years. In the past, the main genetic tests searched for abnormal chromosome numbers and mutations that lead to rare, inherited disorders. Today, tests involve analyzing multiple genes to determine the risk of developing certain more common diseases such as heart disease and cancer. The results of a genetic test can confirm or rule out a suspected genetic condition or help determine a person's chance of developing or passing on a genetic disorder. Several hundred genetic tests are currently in use, and more are being developed.Because genetic mutations can directly affect the structure of the proteins they code for, testing for specific genetic diseases can also be accomplished by looking at those proteins or their metabolites, or looking at stained or fluorescent chromosomes under a microscope.This article focuses on genetic testing for medical purposes. DNA sequencing, which actually produces a sequences of As, Cs, Gs, and Ts, is used in molecular biology, evolutionary biology, metagenomics, epidemiology, ecology, and microbiome research.
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