Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- define terms Euchromatin and heterochromatin euploidy and aneuploidy (with examples) mosaicism uniparental disomy trisomy rescue auto allopolyploidyarrow_forwardWhich of the following statements regarding gene duplication are FALSE? Select ALL that apply. extra gene copies are highly deleterious duplications arise through unequal crossing over duplicates in the same gene family are called paralogs duplication is an important source of new genes duplications confound the pairing of homologous chromosomes, leading to fertility problemsarrow_forwardA reciprocal translocation results from an exchange of chromosomal material between: O non-homologous chromosomes O non-homologous genes homologous genes O alleles O non-homologous genesarrow_forward
- What chromosome rearrangement is thought to be the source of new genes?arrow_forwardDescribe how errors in chromosome structure occur through inversions and translocationsarrow_forwardWhich of the following is false? Group of answer choices With a pericentric inversion, there is no loss in genetic material. Haploinsufficiency is caused by a duplication event causing increased expression of a gene. An effect of aneuploidy is that it changes the dosages of some genes. Pseudodominance indicates that one of the homologous chromosomes has a deletion. Sterility is a possible effect of autopolyploidyarrow_forward
- A chromosome initially has the following segments:A B • C D E F G Draw the chromosome, identifying its segments, that would result from the following mutations. Q. Paracentric inversion that includes DEFGarrow_forwardBriefly explain how transposition causes mutations and chromosome rearrangements.arrow_forwardWhich process can cause duplications? misalignment of homologous chromosomes at repetitive sequences followed by crossing over repair of a double-strand break by homologous recombination a mutagen that introduces point mutations repair of two double-strand breaks that occur in the same chromatid by nonhomologous end-joiningarrow_forward
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