माइक्रोडिलीशन सिंड्रोम

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माइक्रोडिलीशन सिंड्रोम है जो अनेक जीनों में फैले 5 मिलियन बेस पेयर (5 एमबी) से छोटे क्रोमोसोमल डीलेसन (आनुवांशिकी) के कारण होता है जो पारंपरिक साइटोजेनेटिक उपाय या उच्च रिज़ॉल्यूशन कैरियोटाइपिंग (2-5 एमबी) द्वारा ज्ञात करने के लिए बहुत छोटा है।[1][2] जांच फ्लोरसेंस इन सीटू हाइब्रिडाईजेशन (फिश) द्वारा की जाती है। कैरियोटाइपिंग विधि का उपयोग करके बड़े क्रोमोसोमल विलोपन सिंड्रोम का पता लगाया जा सकता है।

उदाहरण


संदर्भ

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