Biology 1201A Study Guide - Midterm Guide: Sister Chromatids, Homologous Chromosome, Aneuploidy

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2 Apr 2018
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Interpret a karyotype for haploid number, ploidy, chromosomal disorders, gender and/or provide possible explanations for novel karyotypes. Haploid number would be one set of chromosomes (n = 23) and we are diploid because we have. 2 sets of chromosomes; we do have polyploid human cells and these are found in liver cells. A karyotype is the number of nuclear genome = 23 pairs of chromosomes lined up for humans. The last 23rd set of chromosomes are called the sex chromosomes: if a human has xx chromosome, it is female; if the human has an xy, it is a male. Understand the link between dna structure, genotype and phenotype and use this knowledge to interpret novel situations/information. Dna is coiled up into chromosomes by histone proteins and within those chromosomes, there are sections that are called genes each gene contains information necessary to synthesize i(cid:374)di(cid:448)idual (cid:272)o(cid:373)po(cid:374)e(cid:374)ts of a(cid:374) orga(cid:374)is(cid:373)"s (cid:272)ellular (cid:373)a(cid:272)hi(cid:374)ery.

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