COP1 is found in the nucleus in the dark and in the cytoplasm in the light.

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#Id: 2074

#Unit 8. Inheritance Biology

Persons with Klinefelter syndrome have a Y chromosome and two or more X chromosomes in their cells such as XXY, XXYY, XXXY and XXXXY.

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#Id: 2075

#Unit 8. Inheritance Biology

More than two X-chromosome causes Poly-X female and Triplo-X

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#Id: 2076

#Unit 8. Inheritance Biology

During human chromosome rearrangements deletion onto the chromosome 5 in the short arm causes Cri-du-chat syndrome.

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#Id: 2077

#Unit 8. Inheritance Biology

During human chromosome rearrangements deletion onto the chromosome 4 in the short arm causes Wolf–Hirschhorn syndrome.

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#Id: 2078

#Unit 8. Inheritance Biology

During human chromosome rearrangements deletion onto the chromosome 7 in the long arm causes Williams–Beuren syndrome.

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#Id: 2079

#Unit 8. Inheritance Biology

During human chromosome rearrangements deletion onto the chromosome 15 in the long arm causes Prader–Willi syndrome.