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The abnormality in patient A was _________ found in ________ chromosome. Based on this evidence and ________ in the history patient A most likely has _____ genetic disorder. **Answers can also include possible symptoms of the disorder, any statistics you found, etc.

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The abnormality in patient A was an extra chromosome found in chromosome 21. Based on this evidence , patient A most likely has downs syndrome.

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the abnormality in patient b was that he had a extra Y chromosome based on the evidence and his infertility he most likely has Klinefelter's Syndrome which one of the symptoms being infertility

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The abnormality in patient A was the fetus had an extra chromosome  found in the 21st set of chromosomes. This patient will have down syndrome.

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The abnormality in patient A was that the fetus had an extra chromosome in set 21. The patient has klinefelters syndrome.

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the abnormality in patient C was trisomy found in 13 chromosome. based on this evidence and symptoms in the history patient C most likely has trisomy 13 syndrome

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I think the abnormality in patient B is that she had an extra chromosome which was a Y. She is diagnosed her having klinefelter
syndrome

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The abnormality in patient A was that the patient had an extra chromosome in chromosome set 21. Based on this evidence and the patients karyotype . Patient A has down syndrome

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The abnormally in patient A was it had a extra chromosome found in the chromosone the patient has down sydrome genetic disorder .

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Patient A had an extra chromosome out of 21. Patient A most likely has down syndrome genetic disorder

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The abnormality was an extra chromosome found in the  sex chromosome. Based on this information, the patient most likely has Klinefelter's Syndrome.

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patient A had a extra chromosome that could lead that person into having down syndrome

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The abnormality is the extra chromosome Y. Which means they have klinefelters syndrome.