Achondroplasia,is characterized by difficulty converting cartilage to bone and thus results in shortened limbs. This trait is autosomal dominant. (A = achondroplasia allele; a = average height allele.) A husband and wife both have achondroplasia. The couple have a total 12 living children: 6 boys and 6 girls.  The husband is colorblind, which is an X-linked recessive trait, and the wife believes there is a chance she is a carrier of colorblindness, since that trait runs in her family. One of the couple’s daughters and three of their sons are colorblind.  (Xc = colorblindness allele; XC = normal color vision allele.) a) Please list all of the different gametes that the husband can produce. b) Please list all of the different gametes that the wife can prod

Q: Hemophilia is a typical example of Sex-Linked Inheritance. If the man is hemophilic and marries a…

A: Haemophilia is also known as bleeder's disease. This disease was first studied by John otto in the…

Q: Amelogenesis imperfecta (AI) is a disorder of faulty tooth enamel formation. It is inherited in an…

A: Amelogenesis imperfecta A faulty tooth enamel formation. Dominant traits Autosomal dominant allele…

Q: cance of color blindness in humans is due to a recessive gene located on the X chromosome X linked).…

A: Mother     ×      father            XXc                  XcY Progeny -      X Xc Xc XXc…

Q: Cystic fibrosis (f) and deafness (d) are caused by two unlinked autosomal recessive alleles, and…

A: Cystic fibrosis (f) and deafness (d) are caused by two unlinked autosomal recessive alleles, and…

Q: Hemophilia affects men much more than women. However, some women can be affected. The hemophilia…

A: Haemophilia is X linked recessive disease.  It is abnormal bleeding  disorder in which blood doesn't…

Q: A man with red-green color blindness marries a woman who is not color blind. They have 3 children,…

A: Color blindness is basically a genetic disorder which can be inherited from parents.These patients…

Q: In this part, you will work out on X-linked traits. Remember that males have only one X chromosome…

A: Pedigree is a diagram which helps to understand the inheritance of a trait across generations in a…

Q: An unaffected man and an unaffected woman mate and have a son affected with Kakamania. Which of the…

A: Answer: Chromosomal Inheritance is the process of transferring the genetic information from parents…

Q: Achondroplasia, which is characterized by difficulty converting cartilage to bone and thus results…

A: Hhsbanf is colorblind i.e XcY  Wife is carrier as their son and daughter both are affected .i.e XCX…

Q: A couple is both heterozygous for the autosomal recessive disease cystic fibrosis (CF). What is the…

A: Autosomal recessive inheritance pattern is a type of inheritance pattern in which the disease is…

Q: Amelogenesis imperfecta (AI) is a disorder of faulty tooth enamel formation. It is inherited in an…

A: The trait shown is inherited both autosomal dominant and X-linked; the presence of the dominant gene…

Q: Julie (a female) has hemophilia. Based on this information, what can we say about the genotypes of…

A: Introduction X-linked diseases are those that occur due to the presence of abnormal/ diseased…

Q: Both red/green color blindness (R=normal, r=colorblind) and Duchenne-type muscular dystrophy…

A: X-linked recessive inheritance is the genetic condition that can be passed from parent to child…

Q: Which genotype indicates a carrier of an autosomal recessive trait?   bb   BB   Bb

A: The dominant allele (represented by capital letter  'B' )  can show its character in the phenotype…

Q: A form of hemophilia is caused by a sex-linked (X-linked) recessive gene. A phenotypically normal…

A: 50 percent chances.

Q: Two affected daughters and two normal sons are born to an affected male and a normal female. Each of…

A: The pedigree analysis helps us identifying the mode of inheritance of a particular disease and it…

Q: Achondroplasia, which is characterized by difficulty converting cartilage to bone and thus results…

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

Q: Considering a common autosomal recessive trait: (Read each statement carefully. Select all of the…

A: Autosomal recessive: In this type the gene or condition is recessive type which means expressed in…

Q: The gene for polydactyly (P) is autosomal and dominant to normal fingers (p). Hemophilia is…

A: Genes are specific regions in the DNA that code for specific proteins. The genetic instructions…

Q: An individual that is genetically male develops as a female. Is this individual more or less likely…

A: The males have one X chromosome and one Y chromosome and the females have a pair of X chromosomes.…

Q: Review the process of autosomal dominant inheritance by coloring the following figures. In this…

A: According to the question, we have to review the process of autosomal dominant inheritance by…

Q: Constructing and Using a Pedigree Duchenne's muscular dystrophy (DMD) is a well known, lethal…

A: A pedigree chart is a graphic that depicts the incidence and emergence of phenotypes of a gene or…

Q: Greg and Susan have Nail- Patella syndrome (NPS). NPS is an autosomal dominant. Greg has a blood in…

A: Introduction  The nails, knees, elbows, and pelvis are abnormal in people with nail-patella…

Q: In humans, hemophilia is a sex-linked recessive disease, and the gene is located on the X…

A: Hemophilia is a sex-linked recessive disease. This means that in order to produce a diseased…

Q: dominant that is 80% penetrant. Clara inherited her polydactyly from her mother, her father had no…

A: 80% penetrant means that in spite of the presence of the dominant allele still 20% people would not…

Q: In humans, blue eyes are inherited as a recessive autosomal trait and color blindness is an X-linked…

A: The objective of this question is to determine the probability of this couple having a son with…

Q: Wilma and Wally have one male child who has been diagnosed withDuchenne muscular dystrophy, an…

A: Duchenne muscular dystrophy is a medical condition of muscular dystrophy which is caused by DMD gene…

Q: Amelogenesis imperfecta (AI) is a disorder of faulty tooth enamel formation. It is inherited in an…

A: Genes are the unit of inheritance that transfers traits from one generation to another. Genes coding…

Q: Albinism and sickle cell anemia are both autosomal recessive disorders that are expressed only in…

A: Albinism - genotype be A and a.  aa is diseased, Aa is the carrier and AA is not affected.  Sickle…

Q: Albinism is an autosomal recessive condition characterized by absence of melanin pigment from the…

A: Albinism is a group of genetic disorders characterized by a lack of melanin, the pigment that gives…

Q: Charles has achondroplasia dwarfism (autosomal dominant) but his wife is normal. What is the…

A:

Q: While studying of the family tree with history of hypertrichosis (hyper hirsutism of the ear) this…

A: Introduction :- Hypertrichosis, which can affect both men and women, is described as excessive hair…

Q: Hemophilia is a X-linked genetic disorder causing blood clotting problem. A dominant allele on the X…

A: The alleles are generally of dominant and recessive type and some other forms like codominant are…

Q: Suppose gene B is X-linked and is embryonically lethal when homozygous or hemizygous recessive. A…

A: Let us first discuss the terms used in the question, Homozygous:- A condition when two copies of an…

Q: Color blindness is an X-linked recessive disease. A female and a male with normal vision have 4…

A: The failure to discriminate between red and green colors is the most common symptom of color…

Q: Tightly curled hair is caused by a dominant autosomal gene in humans. If a heterozygous curly-haired…

A: The major traits of Autosomal inheritance is : trait should not skip generations as well as the…

Q: Duchenne Muscular Dystrophy is an X-linked recessive disease. A couple is wanting to have a child.…

A: Duchenne muscular dystrophy is the most common childhood form of the disease; it occurs in one of…

Q: Consider the following pedigree, which traces the inheritance of a single-gene hereditary disease.…

A: Single gene herediary diseases are mainly caused by a change of any one gene in a particular DNA.Its…

Q: Amelogenesis imperfecta (AI) is a disorder of faulty tooth enamel formation. It is inherited in an…

A: Amelogenesis imperfecta (AI) is a disorder of faulty tooth enamel formation. It is inherited in an…

Q: Red-green color blindness is an X-linked recessive disorder. If Allison is heterozygous (a carrier),…

A: The X-linked genes show a different pattern of inheritance in males and females. The male progeny…

Q: Haemophilia is an X-linked recessive disorder. If a woman is a carrier for haemophil. and has a…

A: Hemophilia is basically an inherited bleeding disorder in which the blood doesn't clot properly,…

Q: man with male pattern baldness, which is a recessive gene, marries a woman who is a carrier of this…

A: Cross is always done in a punett square. The recessive character is only expressed in humans as…

Q: Piebaldism is a skin condition that causes an infant to be born with white birthmarks due to a…

A: It is an autosomal dominant genetic disorder. It is mainly due to the absence of melanocytes of the…

Communication

Communication is a method of transferring information between two persons or organisms. Communication is possible using mutually understood behaviors such as signs, symbols, or language. In the year 1980, S. F. Scudder proposed communication theory. According to his ideas, all living beings on the earth communicate, but the methods of communication differ. Communication skills are now part of soft skills.