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How is the early diagnosis of genetic diseases usually done?
Genetic disease might be diagnosed in the prenatal period by karyotype analysis, in case of aneuploidies, or by DNA analysis, in case of other diseases.
The test is done by removal of material containing cells of the embryo by amniocentesis (extraction of amniotic fluid) or cordocentesis (puncture of the umbilical cord) or even by chorionic villus biopsy.
Define Water - Important Nutrient? Macronutrients, you know, are those nutrients which are required in large amounts by our body namely, carbohydrates, fats and proteins. We st
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Specific Gravity The density of a substance is defined as mass per unit volume. The density of a substance is a characteristic property and has a definite value at a given te
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Define the Parenteral Nutrition Support? Parenteral nutrition support is the provision of dextrose, amino acids, electrolytes, vitamins, minerals and trace elements with or wit
what are the biological significance of the skeleton?
Explain about the Saponins? These are a diverse group of compounds commonly found in legumes like soybean, lentils, chickpeas, peanuts and alfalfa sprouts. They are also presen
How ecosyestem concept is useful to the study of environment?
Explain Ventilation (NIV)? This refers to the use of mechanical ventilatory support without the use of an endotracheal tube. NIV may be by the application of a continuous posit
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