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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.
Determine the term - Leuconoid sponge. The most complex of the three different sponge architectures. Choanocytes are found in chambers, and there is not any spongocoel. Water e
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Q. Use of Neurotensin in consciousness? Although little is known about the role of this peptide during the sleep-wake cycle, it has recently been shown that neurotensin injecti
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Body systems and organs and their functions The human body is a large structural unit made up of many smaller parts. There are four kinds of smaller units - cells, tissues, org
Immediate Post-operative Care The patient is accompanied to the ICU by a surgeon, anesthetist and the nurse who assisted for the surgery with portable ventilator and ECG
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