der(X) der(22) 22 der(X) 22 der(X) 22 First row is mother, second row is first daughter, third row is second daughter. Phenotype in first daughter was much more severe than second daughter. Give best explanation: O Inactivation in second daughter spread to the extra chromosome 22 segment O Having 45 chromosomes always gives a more severe phenotype than 46 chromosomes O Pattern of inactivation in other tissues, including brain might differ, giving functional 22q monosomy The presence of the third X in the second daughter decreases effect of genetic abnormality First daughter has a Turner-like syndrome, which explains severity ..---------- --------- -------------- 7------- L------------- ---------- . Ix ------

der(X) der(22) 22 der(X) 22 der(X) 22 First row is mother, second row is first daughter, third row is second daughter. Phenotype in first daughter was much more severe than second daughter. Give best explanation: O Inactivation in second daughter spread to the extra chromosome 22 segment O Having 45 chromosomes always gives a more severe phenotype than 46 chromosomes O Pattern of inactivation in other tissues, including brain might differ, giving functional 22q monosomy The presence of the third X in the second daughter decreases effect of genetic abnormality First daughter has a Turner-like syndrome, which explains severity ..---------- --------- -------------- 7------- L------------- ---------- . Ix ------

Name: ofder(X) der(22)22der(X)22der(X)22First row is mother, second row is
Uploaded: 2024-03-20T06:43:04.000Z
Channel: Bartleby
Description: ofder(X) der(22)22der(X)22der(X)22First row is mother, second row is first daughter, third row is second daughter.Phenotype in first daughter was much more severe than second daughter.Give best explanation:O Inactivation in second daughter spread to

Biology: The Unity and Diversity of Life (MindTap Course List)

15th Edition

ISBN:9781337408332

Author:Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr

Publisher:Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr

Chapter14: Chromosomes And Human Inheritance

Section: Chapter Questions

Problem 5GP: Human females have two X chromosomes (XX); males have one X and one Y chromosome (XY). a. With...

See similar textbooks

Similar questions

A colleague e-mails you saying that she has identified an interesting chromosome variation at 21q13. In discussing this discovery with a friend who is not a cytogeneticist, explain how you would describe this location, defining each term in the chromosome address 21q13.
A normal female is discovered with 45 chromosomes, one ofwhich exhibits a Robertsonian translocation containing most ofchromosomes 18 and 21. Discuss the possible outcomes in heroffspring when her husband contains a normal karyotype.
1. 10 Meiosis Reading and Voc X James Green- Recovery Opportu X d/e/1FAlpQLSe2TqFrpPuk-re3-isqbyWK6SUIH3pkHhJdbT0tlqogh58bww/viewform?hr_submission=Chkis-WD4ZSE What is the process by which haploid gametes combine, forming a diploid 3p cell with 2n chromosomes, with n chromosomes from the female parent and n chromosomes from the male parent? Topography O Fertilization Genomics Crossing over 2 points nit that controls inherited trait expression that is passed II
Somatic cells in organisms of a particular diploidplant species normally have 14 chromosomes. Thechromosomes in the gametes are numbered from 1through 7. Rarely, zygotes are formed that containmore or fewer than 14 chromosomes. For each of thezygotes below, (i) state whether the chromosomecomplement is euploid or aneuploid; (ii) provideterms that describe the individual’s genetic makeupas accurately as possible; and (iii) state whether ornot the individual will likely develop through theembryonic stages to make an adult plant, and if so,whether or not this plant will be fertile.a. 11 22 33 44 5 66 77b. 111 22 33 44 555 66 77c. 111 222 333 444 555 666 777d. 1111 2222 3333 4444 5555 6666 7777
in the experiment of following chromosomal dna mvement througgh meiosis, why. do you use non-sister chromatids to demobstrate crossing over? what combinatiobns of alleles could result from a crossover between BD and bd chromosomes? Identify two ways that meiosis contributes to genetic recombination. Why is it necessary to reduce the number of chromosomes in gametes, but not in other cell?
2n = 2 pairs of G1 SG2 homologous chromosomes Skip prophase I, do not draw crossing over Metaphase I Draw nondisjunction happen to 21 Anaphase | Metaphase II Anaphase II Telophase II & egg formation 2n = 2 pairs of G1 G2 homologous chromosomes 14 S Skip prophase I, do not draw crossing over Metaphase I Draw nondisjunction happen to 21 Anaphase I Metaphase II Anaphase II Telophase II & egg formation Label which chromosome of mono/trisomy. Which zygotes are aborted? G2 G1 ос old & Zygote formation, add a normal sperm cell to each egg below OOOO
A sexually reproducing organism has the following phenotype DdEeAaTt: The D and E loci are on the same arm of a metacentric chromosome in cis configuration. The A locus is on the long arm of an acrocentric chromosome and the T locus is on a telocentric chromosome. There are no other chromosomes. 1. What is the haploid number of this organism? 2. Using diagrams, show a cell at metaphase of mitosis and show the results of mitosis. Ensure you show the location of the gene loci on the different chromosomes.
Draw and label the mitotic phases (prophase, metaphase, anaphase & telophase) and meiotic phases (prophase I, metaphase I, anaphase I, telophase I, prophase II, metaphase II, anaphase II, & telophase II) for 2N=6. Be sure to indicate the chromosomal complement at each stage and whether the chromosomes are duplicated (consisting of sister chromatids) or not. For the meiotic phases, please add the following labels to your diagrams: In prophase I: tetradIn metaphase I: nonsister chromatidsIn anaphase I: homologous chromosomes, kinetochore microtubule In telophase I: sister chromatidsIn prophase II: centriolesIn metaphase II: centromereIn anaphase II: nonkinetochore microtubule, astral raysIn telophase II: cleavage furrow
An individual heterozygous for a reciprocal translocation possesses the following chromosomes: A B ● C D E F G, A B • C D V W X, R S •T U E F G, R S•T U V W Xa. Draw the pairing arrangement of these chromosomes in prophase 1 of meiosis. Mention their gametic composition. b. Draw the alternate, adjacent I, and adjacent II segregation patterns in anaphase I of meiosis. Mention their gametic composition.
10:10 E ← sisAndMeiosis.docx FREE EDIT PDF FREE CONVERT PDF TO WORD 2. Why are chromosomes important? 3. How are meiosis I and meiosis II different? 1. What is the state of DNA at the end of meiosis I? What about at the end of meiosis II? 4. Why do you use non-sister chromatids to demonstrate crossing over? 7. Identify two ways that meiosis contributes to genetic recombination. 10. P FREE PDF FILLER 5. What combination of alleles could result from a crossover between BD and bd chromosomes? 8. Why is it necessary to reduce the number of chromosomes in gametes? 6. How many nuclei are present at the end of meiosis II? How many chromosomes are in each? a. Sperm Cell b. Egg Cell AP_5 c. Daughter Cell from Mitosis ON 5G I 9. Blue whales have 44 chromosomes in every cell. Determine how many chromosomes you would expect to find in the following: d. Daughter Cell from Meiosis II COUS ra PAGE 10... FREE CONVERT JPG TO PDF X OeScience Labs, 2016
What would be the amount of DNA picograms during Prophase I, Metaphase I, Anaphase I and after Cytokinesis during Meiosis I for a diploid (2n=4)?
A sexually reproducing organism has the following phenotype DdEeAaTt: The D and E loci are on the same arm of a metacentric chromosome in cis configuration. The A locus is on the long arm of an acrocentric chromosome and the T locus is on a telocentric chromosome. There are no other chromosomes. Using diagrams, show a cell at metaphase of mitosis and show the results of mitosis. Ensure you show the location of the gene loci on the different chromosomes.