Biology

Biology, 19.07.2019 11:00, kevincaleb1

If geneticist were to examine closely the makeup of a singe autosomal chromosome from one of your cells that chromosome would be found to be

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Biology, 13.07.2019 00:30, damariush567

Assume that during meiosis i, none of the c chromosomes disjoin at metaphase, but they separate into dyads (instead of monads) during meiosis ii. each resultant gamete participated in fertilization with a normal haploid gamete. what combinations will result? check all that apply. check all that apply. two copies of chromosome a, one copy of chromosome b, three copies of chromosome c two copies of chromosome a, two copies of chromosome b, two copies of chromosome c two copies of chromosome a, two copies of chromosome b, one copy of chromosome c two copies of chromosome a, two copies of chromosome b, three copies of chromosome c one copy of chromosome a, two copies of chromosome b, three copies of chromosome c two copies of chromosome a, two copies of chromosome b two copies of chromosome a, two copies of chromosome b, four copies of chromosome c two copies of chromosome a, two copies of chromosome b, five copies of chromosome c

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Biology, 21.08.2019 19:00, leo4687

How many and what type of chromosomes would be expected in a karyotype of a human male? (1 point) 22 pairs of autosomal chromosomes and 2 y chromosomes 23 pairs of autosomal chromosomes and 2 y chromosomes 22 pairs of autosomal chromosomes, 1 x chromosome, and 1 y chromosome 23 pairs of autosomal chromosomes, 1 x chromosome, and 1 y chromosome

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Medicine, 29.08.2019 23:30, AutumnJoy12

Genes described as sex-linked are located: a. on the y chromosome b. on the x chromosome c. on all autosomal (non-sex) chromosomes d. only in the cells of females e. only in the cells of males

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Biology, 08.10.2019 21:00, bigchriss

Which mutations can a geneticist identify with the g‑banding technique? (a) a nonsense mutation introducing a premature stop codon into a gene on chromosome 5(b) a reciprocal translocation of parts of chromosome 1 and chromosome 11(c) a translocation of a region of the short arm between sister chromatids(d) a deletion of half of the long arm of chromosome 20 a single nucleotide(e) substitution in which t replaces c on chromosome 2

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