Trait W is found in the individuals represented by the shaded symbols in the following pedigree. Trait W is rare in the general population. Which of the following patterns of transmission is consistent with this pedigree? Select one: a. Autosomal recessive b. X-linked dominant c. X-linked recessive d. Autosomal dominant

Q: The pedigree follows the inheritance of a relatively common trait.  Is the trait most likely…

A: A pedigree chart depicts the family members who are impacted by a genetic trait and a family tree.…

Q: In humans, four different blood types (A, B, AB, and O) are encoded by three alleles 1. I. and &…

A: Antibodies and antigens are types of blood proteins that vary from person to person. Antigens are…

Q: Fragile X syndrome is an X-linked recessive Achondroplasia is an autosomal dominant trait…

A: Gene expression

Q: Marfan’s syndrome is an example of pleiotrophy where individuals with a copy of the dominant allele…

A: It is an inherited disorder that  affects the connective tissues of the body. It is  caused by a…

Q: In humans, the genetic disease cystic fibrosis is caused by a recessive allele (a). The normal…

A: Cystic fibrosis is only caused when both of the mutant alleles for cystic fibrosis are present. AA…

Q: 1 2 II 2 3 4 5 6 7 8 III 1 2 3 4 5 6 7 8 9

A: Huntington's disease is an autosomal dominant disease which means only one allele would suffice to…

Q: In human beings, the gene for red‑green colorblindness (r) is sex‑linked and recessive to its allele…

A: normal vision male =XR Ycolor blind male= XrYnormal vision female= XR XRcolorblind female =Xr Xr…

Q: What is the pattern of inheritance? Please Provide a specific reason that justifies your selection…

A: Pattern of anheritance could be autosomal or sex linked..Autosomal   inheritance means that the…

Q: Cats also have a locus (gene) for a character called agouti. In cats with agouti fur, pigment is…

A: Given :    Agouti allele is dominant to the allele for normal fur.  Let's assume ' A ' for dominant…

Q: this disorder? (Is it autosomal dominant? Autosomal recessive? X-linked dominant? X-linked…

A: Inheritance inheritance is described as a pattern of transfer of genes from the parental generation…

Q: Pompe disease is a glycogen storage disorder caused by a lack of ⍺-glucosidase, the enzyme that…

A: Introduction  A rare disorder called glycogen storage disease (GSD) affects how the body consumes…

Q: Ichthyosis is a rare X-linked recessive disorder that is characterized by scaling of the skin around…

A: X linked recessive disorder or inheritance implies that their is a mutation in the genes of X…

Q: A pedigree analysis was performed on the family of a man with schizophrenia. Based on the known…

A: Schizophrenia is a mental disorder wherein the affected individual is unable to interpret reality…

Q: I. II. III. 1 1 2 2 ? 3 3 In the pedigree above, there could be carriers that are not marked. For…

A: PEDIGREE ANALYSIS: The analysis of the diagram or chart that represents a family's genetic history…

Q: In addition to the allelic pair determining pattern baldness in man (B,b), consider early baldness…

A: Introduction  Inheritance is referred to as the transfer of character from parents to offspring and…

Q: In humans, cystic fibrosis and albinism are both inherited as independently assorting autosomal…

A: The law of independent assortment was first observed by Gregor Johann Mendel in 1865 during his…

Q: 6) For the pedigree shown below, answer the following questions. I II II I a) What type of…

A: Pedigree analysis helps us identifying the mode of inheritance of a particular disease by observing…

Q: lease consider the following pedigree. Assume that people who marry in to the family do not carry…

A: The pedigree indicates if the DNA is passed down unchanged from generation to generation. It can…

Q: Without referring to the notation used to write the genotypes, how are you able to tell that a gene…

A: All these are defined by the Alleles they inherit and the type of phenotype they show  These can be…

Q: Tuberous Sclerosis (TS) is an autosomal dominant genetic disease characterized by seizures, mental…

A: Tuberous sclerosis is a rare autosomal dominant disease that causes non-cancerous tumors in various…

Q: Skin color in humans is determined by polygenic inheritance, which means the more dominant alleles…

A: Polygenic inheritance: - in this inheritance, more than one genes control the single characteristic.…

Q: Sickle cell anemia is inherited as an autosomal recessive condition. It also exhibits incomplete…

A: Sickle cell anemia (SCA) is a genetic disorder that occurs when an individual has two homozygous…

Q: Below is a pedigree of a human genetic disease in which solid color indicates affected individuals.…

A: In the given pedigree, atleast one member in all generations have the disease. Therefore,…

Q: Hypophoshatemia is a dominant genetic disorder caused by deficiency of pho[hates in the blood.…

A: The pattern of inheritance in question involves a genetic disorder related to phosphate deficiency…

Q: You possess two alleles for each of your genes. (One from the paternal side and one from the…

A:

Q: Determine what is the most likely mode of inheritance of this disease (whether it is inherited as…

A: Inheritance pattern is a pattern tat evaluates how traits are transmitted from parent generation to…

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.