Identify the following chromosomal mutations.

Q: List the diagnostic features (genetic or cytological) that are used to identify these chromosomal…

A: In the nucleus of a cell – DNA is present in the form of chromosomes. These are compact structures…

Q: Please write in digital format Define the following terms: a) Triploid b) Monosomic c) Trisomic d)…

A: Normal cell has a diploid number of chromosomes. Each cell has 23 pairs of chromosomes out of which…

Q: Please explain why chromosomal inversions are less detrimental to the organism than a duplication…

A: DNA is the genetic material in most living organisms. It is the information hub of the cell that…

Q: In 1-3 sentences define Sense, Missense, Nonsense mutations, Frameshift mutations, Allelic…

A: The cell is the basic structural and functional unit of life. It carries out various functions in…

Q: What is reverse tandem duplication?

A: Duplication is a type of mutation, which involves the production of one or more copies of a gene or…

Q: In Figure 4-9, why is only locus A shown in a constantposition?

A: Genes are present on the chromosomes in the linear order.

Q: Chronic myelogenous leukemia is usually associated with which type of chromosome rearrangement? a.…

A: Genetics is the branch of biology which deals with genes, heredity, and genome in the organism.…

Q: Both karyotyping and G_banding techniques show normal chromosomal pattern, however pedigree analysis…

A: Answer: Introduction: A pedigree shows the pattern of inheritance of a particular trait in entire a…

Q: What causes monosomy and trisomy disorders? deletion insertion translocation O non-disjunction

A: Monosomy and trisomy-  Monosomy = It is the type of aneuploidy when only one chromosome of a pair is…

Q: Animation 12.1: This table shows results from allele specific oligonucleotide hybridization analyses…

A: Blotting techniques are the methods used in the molecular biology for the identification or…

Q: Cystic fibrosis (CF) is an autosomal recessive disorder. Several different individual point…

A: Cystic fibrosis is a disease of the mucus secretion in which thick viscid mucus is secreted which…

Q: Familial Down Syndrome is an inherited trait that is caused by ____________________________.…

A: Down syndrome is also known as trisomy 21 which is caused by the extra number of chromosome.

Q: Define deletion-insertion polymorphisms (DIPs)

A: Insertion is a mutation in which one or more nucleotide base pairs are added into a DNA sequence.…

Q: Duplication Inversion Deletion

A: Gene mutations are rare and random changes in DNA sequence which result in alteration of polypeptide…

Q: The image shows the karyotype of someone suffering from Patau syndrome. 2 3 4 5 6 7 8 10 11 12 13 14…

A: Answer b- chromosome set 13. In This karyotype there is an extra copy of chromosome 13.

Q: D3S1358 130 14 517 18 503 The DNA locus pictured is considered homozygous inconclusive a mixture…

A: DNA locus It is defined as the specific location of a particular gene or other sequence of DNA on a…

Q: the deletion of which chromosome causes obvious morphological and mental defects in the organism,…

A: Cri-du-chat syndrome, otherwise called 5p-(5p minus) syndrome or cat cry syndrome, is a chromosomal…

Q: Ir il 9 10 11 12 x* 13 14 15 16 17 18 20 22 Chromosome counts: Karyotype: Interpretation:

A: In human the total chromosome number is 46. Between these 46 chromosomes, 44 chromosomes are…

Q: 13.2 13.1- 12. 11 11- 12 22 23 24 HIDGE b с d f g bo h

A:

Q: name some Variety of Methods Can DetectChromosomal Rearrangements

A: In genetics, chromosomal rearrangement is defined as the chromosomal abnormality that involves a…

Q: Group of answer choices Statement 1 is correct. Statement 2 is incorrect

A: Neurofibromatosis (NF) is a neurodegenerative disease that affects the brain, spinal cord, nerves,…

Q: A male carrier of a recessive somatic mutation marries a female without this mutation. What is the…

A: Recessive somatic mutation is the recessive mutation in the somatic cells of the body that does not…

Q: eueu For each genotype below, select whether it is heterozygous, homozygous dominant, or homozygous…

A: First of all let us check what the terms mean, Heterozygous: It means an organism having two…

Q: If one bit is mutated on the chromosome 11010001, which of the following chromosomes cannot be…

A: * Mutations means change in a DNA sequence by altering the bases. *Mutations arise due to mistakes…

Q: Using the data below please identify the following: Identify which of the siblings in generation II…

A: Adenomatous Polyposis coli (APC) syndrome which is characterized by cancer of large intestine and…

Q: • Deletions remove _______________from a chromosome and causemutant phenotypes mainly through…

A: Mutation is defined as a change which occurs in the sequence of DNA molecule which is due to…

Q: given the photos below, what general type of chromosomal mutation did colchicine induce ? 1st photo-…

A: Colchicine induce polyploidy. Colchicine prevent the microtubule formation during cell division…

Q: Cystic fibrosis (CF) is an autosomal recessive disorder. Several different individual point…

A: Cystic Fibrosis - An hereditary disease that affects the lungs and digestive system and can be…

Q: Match the genetic disorder to the descriptions below: Edward Syndrome Jacob Syndrome Patau Syndrome…

A: Genetic disorders are caused by mutations in the genes and such mutations can be single-gene,…

Q: Nullisomy is a genome mutation where a pair of homologous chromosomes that would normally be present…

A: Chromosomes are long thread-like structures that carry coded genetic information in the form of DNA.…

Q: Name of Abnormality Number of autosomes and sex chromosomes Classification of abnormality…

A: The chromosomal disorder is any syndrome characterized by malformations or malfunctions in any of…

Q: Chorionic villus sampling is a procedure to determine if there are any abnormalities in chromosome…

A: Chorionic villus sampling is also used for the same purpose. Chorion is basically a membrane that…

Q: Cystic fibrosis (CF) is an autosomal recessive disorder. Several different individual point…

A: Answer: #2

Q: Autosomal Dominant is a mutation in one copy of the gene. It is inherited from an affected parent or…

A: One of the ways a genetic trait or a genetic condition can be inherited. In autosomal dominant…

Q: Arrange the correct sequence from 1-13

A: Steps of fertilization process in human- Penetration of corona radiata Sperm attach loosely on zona…

Q: Why is chromosome 21 the smallest and not chromosome 22? considering that a karyogram is arranged…

A: Introduction: In the nucleus of each cell, the DNA molecule is bundled into thread-like structures…

Q: describe a specific example of chromosome abnormality that leads to human cancers, such as leukemia,…

A: Chromosomal aberrations are changes in the number and arrangement of genes in the chromosomes. They…

Q: Alterations of chromosome structure can not be resulted from: اختر احدى الاجابات Translocation…

A: Mutations are  errors occur during DNA synthesis . These errors can be adventageus or dangerous ..…

Q: Both recombination and random fertilization are important for what major biological process? Be…

A: Introduction In Genetics, Recombination Is The Fundamental Process For Introducing Variation Into…

Q: name a disorder  karyotype analysis, pick and explain a disorder associated with a variation in…

A: The example of disorder that can be taken in the current scenario which results from variation in…

Q: Would you be able to draw a circular map of the seven genes? I have trouble with correct position of…

A: The DNA replicates itself several times during the replication process. It is a biological…

Q: What the genetic disease talk about? What cause of the genetic disease?

A: Genetic disease means the disease that is caused by a mutation in the genome and these mutations are…

Q: What is difference between normal primer and degenerative primer

A: Primer: These should be 18–24 nucleotides in the length and it provides for the practical annealing…

Q: What happens when one nucleiotide is lost or changed from the middle of a gene? Describe to me, or…

A: Mutation can happen by environmental factors such as UV radiation from the sun, or can occur if an…

Q: What are the similarities a chromosomal mutation and point mutation?

A: Chromosomal mutation is a numerical or structural change in a chromosome. It causes Klinefelter…