1 2 3 4 5 i、月 6 8 9 10 11 12 13 14 15 16 17 18 19 20 Y 21 22

Q: show the genotype pf all the possible gametes that can be produced by an individual with…

A: Sir Gregor Mendel was a priest and a teacher who did the famous hybridization experiment on garden…

Q: Identify the sex and any genetic conditions by analyzing the karyotype of this individual. 1.a) male…

A: Normal Human body consists of 23 pairs of chromosomes i.e., 46 chromosomes out of which one pair is…

Q: Describe the individuals with the following chromosomal abnormalities: Trisomy at chromosome 21 XXY…

A: Chromosomes are the  condensed forms of chromatin seen during the cell division. They were…

Q: which genetic disorder matches below descriptions. extra 21st chromosome attaches to chromosome 14.…

A: Genetic disorder is defined as the disease caused by the abnormality in the genome of an organism.…

Q: You may include drawings as part of your answers. Explain in detail 2 human chromosomal disorders.…

A: Introduction  Chromosomal aberrations are the common cause of abnormal development of the embryo or…

Q: which genetic disorder matches below descriptions deltetion of part of the Parm of chromosome 5.…

A: It refers to a health problem that can be caused by one or more abnormalities in the genome or by a…

Q: Mode of Inheritance: Phenotype (Normal, Affected, or Carrier) Individual Genotype Sex 1-1 1-2 II -1…

A: Pedigree Chart: A pedigree chart is a diagramatic representation that depicts the incidence and…

Q: Explain about the  Changes in Sex Chromosome Number ?

A: The genetic disorder may occur due to the addition or deletion of chromosomes that will result in…

Q: Interpret the karyotype below for sex and chromosomal abnormalities.

A: The mistake in the meiosis process occurs, where the 21 pair of chromosomes is not able to divide in…

Q: couple contemplating a pregnancy are in today for an appointment at a genetic counselling clinic to…

A: Fragile X chromosome is a genetic condition in which varied developmental disorders are present in a…

Q: Give five sex limited and sex-influenced characters and diagram their possible phenotype and…

A: Sex-limited traits are determined by genes located on autosomes and express only in one sex.…

Q: describe the Major Classes of ChromosomalRearrangements

A: Chromosomal rearrangements are the mutations in the chromosomes that alter the structures of…

Q: 8 9 10 11 12 13 14 15 16 17 18 ir 19 20 21 22 (8) Fig. 6-3, p.123 N CITE

A: Karyotyping is a test to examine chromosomes in a sample of cells. This test can help identify…

Q: Identify the stage of meiosis for the following cells:

A: Since we only answer one question at a time, we’ll answer the first one. Please resubmit the…

Q: Turner syndrome is a disease in which an individual is born with only a single X chromosome. Suppose…

A: Hemophilia is a bleeding condition that is commonly hereditary and affects the way one's blood…

Q: Determine the genotype for each phenotype using the Information provided: SQUARE shape (S) is…

A: *Phenotypes means the traits that an individual contains can be easily observable  * Ex: colour,…

Q: List down 10 human chromosomal aberrations. Give the corresponding karyotype for each type then…

A: Chromosomal aberrations refers to the change in the number and structure of the chromosomes. The…

Q: Explain the nondisjunction event that would cause a Turneror Klinefelter syndrome individual.

A: Nondisjunction refers to the failure of homologus chromosomes or sister chromatid to separate during…

Q: Identify if the description below happens in meiosis, mitosis, or both

A: Mitosis is an equational division in which a parent cell (2n) is  divided into two daughters cells…

Q: B A In the image above, the tissue found at letter B is; Нaploid Diploid Neither

A: The above image belongs to the ferns. It is the prothallus of the fern developed from spores.

Q: Complete what is being asked on the table. Name of the Abnormal Individual The chromosome #…

A: A chromosomal disorder is caused by an abnormal number or constitution of chromosomes. They are…

Q: - Differentiate between autosomal genetic linkage and sex linkage. Criteria Autosomal Genetic…

A: Linkage is the phenomena in which the closely related genes are not segregated instead are inherited…

Q: 2 3 5 8. 10 11 12 13 14 15 16 17 18 19 20 Y 21 22 (4) © 2006 Brooks/Cole - Thomson Fig. 6-18b, p.135

A: KARYOTYPING It is the process by which photographs of chromosomes are taken in order to determine…

Q: tables attached to complete the punnett square   Eye color Parental genotypes: ______ X ______…

A: The alleles are the alternative forms of a gene that are located on the same locus of a homologous…

Q: Identify a disorder caused by a chromosomal abnormality and how the disorder affects the individuals…

A: Chromosomal abnormality are one of the main reasons for many inherited disorders and traits, and…

Q: Match the Term with the appropriate definition. 1: Genome 2: Karyotype 3: Homozygous 4: Heterozygous…

A: A karyotype is a preparation of an entire set of chromosomes. It determines the size, shape, and…

Q: Define multihybrid cross

A: A cross is a controlled breeding experiment in which two organisms of desired or considered trait…

Q: reate a profile of a human chromosomal disorder. the chromosome disorder can be autosomal or sex…

A: Chromosome disorders are the genetic disease in which there is a loss of few sequences or addition…

Q: of Abnormality Number of autosomes and sex chromosomes Classification of abnormality (be specific…

A: Chromosomal disorder is, any syndrome characterized by malformations or malfunctions in any of the…

Q: Individual 14 is thinking of having children, but she knows her family has a history of cancer.…

A: Cancer  It is a uncontrolled growth or cell. Cel divide abnormally and affect other part of body…

Q: What are chromosomal Defects. List and Explain any 5 of them.

A: Almost every cell in our body contains 23 pairs of chromosomes, for a total of 46 chromosomes. Half…

Q: Explain the significance of cleavage lines.

A: A bone is a rigid organ that comprises part of the vertebrate skeleton in creatures. Bones ensure…

Q: Discuss and differentiate: Trisomy 13 Trisomy 18 Trisomy 21 Turner syndrome Klinefelter syndrome

A: Answers All these diseases are genetic disorders. Trisomy 13(2n+1) Also known as Patau syndrome,…

Q: Explain the term double fertilisation.

A: A flower is the reproductive part of the modified thick shoot of an angiosperm plant. In order to…

Q: Examine the following karyotypes and answer the questions about each karyotype in the table below.…

A: Chromosomal abnormalities can occur due to non-disjunction  i.e. a pair of chromosomes fails to…

Q: Indicate below the name of the chromosomal regions that are squared and named respectively A and B…

A: John Cairns was the first person to observe the replicating chromosome in E.Coli by autoradiography…

Q: Define polygenic

A: A trait is any feature of an organism, such as eye color. A phenotype is the set of an organism’s…

Q: 9. 10 11 12 14 15 16 17 18 19 20 21 22 X Y SENA

A: A karyotype is a collection of arrangements and types of chromosomes of an individual. Karyotyping…

Q: Answer the following: a. what environmental factors may increase incidence of chromosomal…

A: Chromosome refers to the long DNA molecule that is located inside the nucleus. It is made of DNA…

Q: Present clinical consequences of most commonly identified numerical chromosome abnormalities.

A: Chromosomes are thread like structures which are found in the nucleus of the eukaryotic cells. In…

Q: For the karyotype featured here, answer the following two questions. 10 12 18 13 14 15 16 19 20 21…

A: Ploidy is a term which describe the number of sets of chromosomes in a cell. The term haploid…

Q: Define these pairs of terms, and distinguish between them. Patau syndrome/Edwards syndrome

A: Some chromosomal disorders are caused due to change in the number of chromosomes in the offspring.…

Q: Using the karyotype and the disorder charts below, which of the following abnormalities is true for…

A: Karyotype:- Karyotyping is the process of matching and ordering all of an organism's chromosomes,…

Q: Compare types of chromosomal abnormalities: numerical vs structural.

A: DNA is considered to be the genetic material within the nucleus that gets packed in thread-like…

Q: Using the Dihybrid Cross, Give the Total Number and Types of Gametes formed.    1. AaBbCCDd  2.…

A: Genotype is considered a genetic combination of traits in an organism. Mandel's law of inheritance…

Mitochondrial Mutations

A mitochondrion is a cellular organelle that serves as the site for cellular respiration and energy production (ATP or Adenosine Triphosphate). It is a double-membrane-bound organelle and is only present in eukaryotic cells.