What is the chance that a child of III-1 and III-4 will have the disease?

Q: Grandma Jade is affected with tuberous sclerosis, she grows benign tumors, and the trait is under…

A: A few people inherit the disorder from a parent with TSC, most cases happen as irregular cases…

Q: A) What is the minimum number of ridge-producing genes possible in one of their children? B) What…

A: Polygenic traits are controlled by two or more genes. Examples of the same are skin color, the…

Q: What would the offspring's blood type be if the mother is type O+ (she is homozygous for Rh factor)…

A: Blood group is determined by the presence of antigen present on red blood cells.

Q: Cystic Fibrosis (CF) is an autosomal recessive condition. Therefore, heterozygous (Cc) carriers do…

A: As a hereditary counselor, we would direct them through the probabilities of their children…

Q: A phenotypically normal man, who has a hemophiliac brother, marries a normal woman, who is not a…

A: Hemophilia is an X-linked recessive disorder so, an individual inherits this disease from his mother…

Q: Hemophilia is a sex-linked recessive trait. A male hemophiliac and phenotypically normal female have…

A: Haemophilia is one of several X-linked recessive hereditary genetic diseases, which occur when the…

Q: stion 10 of 20 Huntington's disease is an inherited autosomal dominant disorder that can affect both…

A: Huntington's disease is a reformist mind issue brought about by a solitary defective gene on…

Q: PKU is an inherited disease caused by a recessive allele. If a woman and her husband, who are both…

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

Q: A man with hemophilia has a daughter of normal phenotype. She marries a man who is normal for the…

A:

Q: what are treatments for polycystic overy syndrome?

A: Polycystic ovary syndrome is the condition of ovary in which the follicles are solidified to form…

Q: In a family, the mother has type A blood, the daughter has type O blood, and the son has type B…

A: ABO blood group shows a codominance pattern. It means that neither of the alleles A or B is…

Q: Explain how it is possible for each baby to be unique:

A: Cells are the biological, structural and functional unit of an organism. Cell has a nucleus that…

Q: Mary, who has type O blood, is expecting a child with her husband Joe, who has type B blood. Joe's…

A: To find what percentage of type O blood their children get.

Q: Jan and Michael are both carriers for the cystic fibrosis allele. If Jan and Michael have five…

A: Introduction Cystic fibrosis (CF) is a genetic disorder, which means it is transferred from…

Q: What term for the baby is used up to 7-8 weeks, and what term is used for the remainder of the…

A: The area of animal biology known as embryology focuses on the formation of gametes in the womb,…

Q: What type of medication for inheritance pattern?

A: In genetics, an inheritance pattern describes the manner in which particular traits or genetic…

Q: A couple, who are both normal, have a daughter who is albino and a son who is normal. a) what is…

A: Albinism has an autosomal recessive disorder and the presence of two recessive mutant genes is…

Q: What is the probability that one of their children would be a carrier? О3/4 O 1/4 O 1/2

A: An allele can be dominant or recessive. The color blindness allele is recessive and X-linked. Thus a…

Q: A boy with cystic fibrosis (a recessive disorder) is born to a couple who appear to be normal. What…

A: Cystic fibrosis is a hereditary, life-threatening disease that affects the lungs and digestive…

Q: Boe is normal and his wife is not color-blind, she is a carrier. Which of the following children…

A: Given  Father is normal Mather is carrier for colour blind trait.    Colour blindness  It is a X…

Q: The percentage chance that the mother described above will give birth to a daughter with mid-digital…

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

Q: Jan and Michael are both carriers for the cystic fibrosis allele. If Jan and Michael have three…

A: Fraternal or dizygotic twins are produced when two different ova are fertilised by 2 different…

Q: Hemophilia is an X-linked recessive disorder that results in an individual not having a functional…

A: The mutation and inheritance of a single defective gene according to the Mendelian principle results…

Q: Two normal visioned parents have a color-blind son. Give the genotype of both parents and the son.

A: Answer: COLOR BLINDNESS = It is the X linked recessive disease which can be transferred from parents…

Inheritance and Mendelian Genetics

Inheritance means the passing of traits to offspring from parents. These traits could be passed either through asexual reproduction or sexual reproduction. The offspring receives the genetic material from the parents. Mendelian inheritance is a certain biological inheritance that follows the rules and principles laid down by Gregor Mendel in 1865. The initial hypothesis was considered wrong, but other inheritance theories modified the concept of inheritance and thus genetics.