Genes that influence a given characteristic and arealigned with one another on a chromosome pair areknown as ___________.

Q: Why most loss-of-function mutant alleles are recessive to wild-type alleles

A: The loss-of-function mutations are also known as inactivating mutations that result in the gene…

Q: A cross was performed between a female curly winged fly and a normal (straight) winged male fly.…

A: As per the question, a cross was performed between a female curly winged fly and a male straight…

Q: What will happen to the person if she/he had more than or less than 46 chromosomes?

A: Each human cell ordinarily has 23 pairs of chromosomes, for a total of 46 chromosomes. A shift in…

Q: Hemophilia results from a sex-linked gene. The disease is most common in males, but the hemophilia…

A:

Q: Explain why it is not possible for two parents, one with type AB blood and the other with type O…

A: Blood group is classified based on the presence and absence of antibodies and inherited antigenic…

Q: To determine: The possible reason for identical twins not having similar and not identical…

A: DNA fingerprinting is a technique for determining the nucleotide sequences of specific areas of…

Q: The genotype XO corresponds to:

A: Genetic disorders are inherited disorders. In genetic disorders, the disorders related to sex…

Q: Duchenne muscular dystrophy, which is inherited in an X-linked recessive pattern, nearly always…

A: Muscular dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass.…

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: O Males and females are affected equally Question 26 Which of the following is a sex-linked…

A: Introduction Genetic disorders are of two types, sex linked and autosomal. Sex linked disorders are…

Q: Duchenne muscular dystrophy is one of the sex-inherited disease. Write a report about the mutation…

A: Duchenne muscular dystrophy (DMD) is a genetic condition that affects the muscles, leading to muscle…

Q: PUNNETT SQUARE: GENOTYPES: BB Bb - bb – PHENOTYPES: Belted -: Non-belted-;

A: A Punnett square is used to understand a typical monohybrid and dihybrid cross conducted by the…

Q: Difference between dominant and recessive genes.

A: difference between dominant and recessive trait  ldefines by genes , dominant genes always passes…

Q: Huntington’s disease is an autosomal dominant disease in humans, but the first symptoms usually…

A: Autosomal dominant disorder inheritance The dominant autosomal mutated gene cause the defect in…

Q: A karyotype shows that a child has Klinefelter syndrome (47,XXY). If the child is also colorblind…

A: Karyotyping is the process of taking photographs of chromosomal pairs to determine the number of…

Q: Explain as you would to a 12th grader why, using Punnett squares the probability an offsprint being…

A: The Punnett square is a graphical representation which displays the potential genotypes of an…

Q: A genetic to lilustrate how a father with blood group A and a mother with blood group B could have…

A: ABO blood grouping was given by Karl Landsteiner in the year 1901. There are basically four blood…

Q: A married couple, both with blood type AB are both carriers of the Bombay trait, are about to have a…

A: Blood help to transport the different nutrients and oxygen through the body. There are mainly four…

Q: What is genetic

A: Genetics is explained as below

Q: You are a doctor who has obtained the karyotype below from a child to be born to one of your…

A: Karyotypes are the actual collection of chromosomes being examined. It is a laboratory technique…

Q: Interpreting the karyotype Lab technicians compile karyotypes and then use a specific notation to…

A: Karyotyping refers to the photographic arrangement of the complete set of individual's chromosome in…

Q: Abnoral changes in chromosome number are often from the failure of chromosomes to separate during…

A: Mitosis is the process by which cell divides into its daughter cells. It consists of karyokinesis…

Q: This question is about a medical condition that is inherited as an autosomal dominant allele. In…

A: Autosomal dominant diseases effect a person even when in heterozygous state but sometimes their…

Q: Briefly explain how McClintock determined that D s was occasionallymoving from one chromosomal…

A: Transposable elements, also known as jumping genes are short segments of DNA, which have special…

Q: difference of ideogram and karyotype

A:

Q: As a genetic counselor, I would recommend Susan and John a blood test for cystic fibrosis. This…

A: Cystic fibrosis screening Pros Early diagnosis for treatment of pancreatic insufficiency Early…

Q: A. What type of abnormality is shown in Lois' karyotype and explain why she does not have a genetic…

A: Introduction A karyotype is the number and appearance of the complete set of chromosomes in the…

Q: Tell me whether it is autosomal reccessive inheritance,autosomal domiant inheritance,sex-linked…

A: Pedigree analysis helps us determine the pattern of inheritance of a trait. In this case the trait…

Q: How many total chromosomes were on your karyotype sheets? How many of the chromosomes are…

A: DNA contains inheritable segments that are called genes that contain instructions for protein…

Q: My Diagnosis for Pati Sex: Chromosomal Disorder Justification:

A: Chromosomes are the parts of your cells that contain your genes. Genes are parts of DNA passed down…

Q: genotypes and phenotypes

A: Genotype:  The genetic make up of an individual is called as the genotype. Example: Eye colour.…

Q: The genotype of an organism with _____________   can be determined from its phenotype.

A: The genotype is a set of genes in DNA responsible for unique characteristic. The phenotype is the…

Q: Examples of genomic imprinting other than insulin-like growth factor 2

A: Genetic imprinting can be defined as when one copy of a gene is silenced due to its parental origin.…

Q: how An inversion can affect phenotype

A: Mutation is the sudden heritable changes that occur in the DNA sequences due to error while copying…

Q: Question 15 Trisomy 21, also known as Down Syndrome, most often occurs because of 1. crossing over…

A: Trisomy 21, also known as Down Syndrome, most often occurs because of nondisjunction. Down syndrome…

Q: Red/green colorblindness X-recessive pedigree

A: Answer: X-linked recessive pedigree is a pedigree chart of a family in which the disease is transfer…

Q: The fundamental unit of heredity is the ___________.

A: Passing down the genetic material by the parents to their next generation is known as heredity. It…

Q: detacched earlobe phenotype and genotypes

A: A genotype is the genetic makeup of an organism. Phenotype is the observable morphological…

Q: Tell me whether it is autosomal reccessive inheritance,autosomal domiant inheritance,sex-linked…

A: To determine the inheritance pattern of any trait we need to do pedigree analysis. Here the trait…

Q: Based on the attached picture Are the blue eye color and white body color mutations located on the…

A: The Drossophila is the widely studied model for inheritance and genetic experiments. The above given…

Q: QUESTION 22 Consider whether the mode of inheritance for each of the pedices below is autosomal…

A: Pedigree analysis is a family chart. It is done to determine the mode of inheritance whether it is…

Q: Multiple Alleles:

A: Given: Gene mutations may produce many different alleles of a gene. Some genes may have as many as…

Q: Gene Allele

A: Genetics is the study of inheritance of traits.

Q: If two unaffected parents have an affected child, they must be what of the gene

A: Given condition:  Two unaffected parents have an affected child.  This is possible only when both…

Q: Gilbert's genetic makeup is homozygous for dark hair. Jan's is homozygous for blond hair. What…

A: Gilbert has genetically dark hair colour. Jan has genetically blond hair colour. Both of them have…

Q: As a genetic counselor, you inform Susan and John that a blood test for cystic fibrosis is…

A: Genetic counselor

Q: What is autosomal cells

A: The autosomes are non gender specific chromosomes or it is not related to sex chromosome. The…

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.