The C-terminal segment of Smo binds Cos2, and Smo is stabilized from degradation

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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.

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#Id: 2080

#Unit 8. Inheritance Biology

Edwards syndrome (trisomy 18) occurs when a person has an extra copy of chromosome 18.

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#Id: 2081

#Unit 8. Inheritance Biology

Burkitt lymphoma possess a reciprocal translocation of c-MYC  gene between chromosome 8 and chromosome 2, 14, or 22

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#Id: 2082

#Unit 8. Inheritance Biology

A reciprocal translocation between the long arm of chromosome 22 and the tip of the long arm of chromosome 9 . This translocation produces a shortened chromosome 22, called the Philadelphia chromosome