Achondroplasia is the most common form of dwarfism in miniature horses. Achondroplasia dwarf horses have normal sized bodies and heads, but noticeably smaller upper legs and ears. This form of dwarfism is an autosomal dominant trait. The pedigree shows the offspring of one horse without dwarfism, Individual 1, and one with dwarfism, Individual 2. The horses with achondroplasia are shorter.

Q: Farmer Brown had two hogs, Olga and Hank.  Olga and Hank were normal, healthy hogs, but whenever…

A: Ogla and Hank must be both heterozygous for the condition. That is why they are producing some…

Q: Fanconi anemia is an autosomal recessive disease caused by a mutation in a single gene. It's a…

A: The objective of the question is to understand how we can determine from a pedigree that Fanconi…

Q: A woman without red-green colorblindness and with a normal chin, whose mother was colorblind,…

A: Genetic inheritance patterns come in two flavors: autosomal dominant and sex-linked recessive. The…

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: The pedigree below describes the inheritance pattern for "muscular atrophy"  determine the mode of…

A: Genotypes of each individual:Note that we used:A = normal allelea = affected alleeDetailed…

Q: The probable mechanism of inhe ince of pedigree is: Autosomal recessive Sex linked dominant OB.…

A: There are several kinds of modes of inheritance of genetic disorders present in humans.

Q: A man, Penoy, whose sister died in early childhood from a recessive lethal disease marries a woman…

A: In the given scenario, as the male survived beyond childhood but is a carrier of the disease, it…

Q: Hair texture is an incompletely dominant trait in humans. The three phenotypes are curly, wavy and…

A: Incomplete dominance which is also known as partial dominance is the trait where-in the phenotype of…

Q: Given in the photo is a family that has a history of phenylketonuria (PKU). Couple 1 Couple 2 PKU…

A: Genes Genes are the sequence in the DNA that code for perticular enzyme or protein.

Q: hair, underdeveloped nails, and abnormally shaped eyelids. In the following pedigree, which…

A:

Q: Consider the cross of a homozygous white & horned male with a homozygous black & hornless female.…

A: Given that white coat (W) is dominant over black coat (w). Also, horns are dominant in males and…

Q: The male is heterozygous for Huntington’s disease and homozygous dominant for Tay-Sachs. The female…

A: Male = Hh TT Female = hh Tt

Q: Using the pedigree chart attached: Above is a pedigree for colorblindness. Based on the pedigree,…

A: Pedigree is a representation in the form of a diagram or family tree of inheritance of genetic…

Q: 1) Symptoms of 4 disorders are listed. Using the lists given, fill in the correct letter for the…

A: Inheritance is a mechanism of the characters, behaviors and traits that are by the another class…

Q: Wilson’s disease is an inherited disorder in which there is too much copper in the body’s tissue. It…

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

Q: A male dog is a carrier for the autosomal recessive disorders centronuclear myopathy (Y/y) and von…

A: Centronuclear myopathy and von Willebrand disease is an autosomal dominant disease and is a single…

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: a) The trait pictured in the pedigree above could follow either of two of the below inheritance…

A: The pedigree being shown is similar to the pedigree of color blindness inheritance.The pattern of…

Q: ased off the information given, complete the table a. What mode of inheritance pattern best fits…

A: A pedigree represents the genetic family history of an individual. It is made of symbols and lines…

Q: Neurofibromatosis-1 (NF1) is an autosomal dominant disorder where tumours form in the base layer of…

A: The probability is 1/4

Q: The pedigree shown below shows the inheritance of cystic fibrosis, a disorder that causes severe…

A: Cystic fibrosis is an inherited disorder that causes extreme damage to the lungs, digestive system,…

Q: Whyte type canaries are yelllow. A dominant mutant allel of the color gene, designated W causes…

A: Introduction :- A genetic disease manifests in autosomal recessive inheritance when one variant is…

Q: Consider an autosomal dominant trait with reduced penetrance and complete expressivity. What might…

A: An autosomal dominant trait is a genetic condition where the presence of a single copy of the…

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: Is this pedigree dominant or recessive. Which best defines this pedigree Autosomal or sex-linked?

A: Introduction :-  A pedigree is a diagram of family history that uses standardized symbols for…

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: 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: Classify the following conditions based on whether they are describing autosomal dominance,…

A: Genetics is a study of genes, heredity, and genetic variation in an organism. Living organisms…

Q: What is the most likely mode of inheritance for the trait shown in the following pedigree? This…

A: This is an autosomal recessive trait.

Q: A man has six digits on each hand and foot (an autosomal dominant trait).  His wife and first…

A: A condition in which an individual has more than 5 digits is known as polydactyly. Polydactyly is an…

Q: For each of the listed modes of single gene inheritance (assuming complete penetrance), indicate…

A: “Since you have posted a question with multiple sub parts, we will provide the solution only to the…

Q: What is the most likely inheritance pattern shown in image B, below? A KEY Homozygous Homozygous…

A: Inheritance pattern is a type of pattern which evaluates how traits are passed from parents…

Q: The second pedigree involves albinism, an autosomal recessive trait.  A couple has a son with normal…

A: A series of genetic illnesses known as albinism (OCA) occur when the pigment melanin is produced…

Q: Your brother has an autosomal recessive disorder, while you are unaffected. Neither one of your…

A: Question - Your brother has an autosomal recessive disorder, while you are unaffected. Neither one…

Q: 1. The pedigree chart in Figure 5.29 shows the inheritance of haemopiu family. Study the pattern of…

A: Solution 1A: GenotypePhenotypeIndividual 2XYNormalIndividual 4XHXHHemophiliac Solution 1b: i)Three…

Q: Consider a cross between a Brown furred dog and a Yellow furred dog. All the puppies born from these…

A: Ans- True Autosomal Recessive Inheritance As in the case of an autosomal recessive trait, it is…

Q: Polydactyly is a condition characterized by extra fingers and/or extra toes. It is caused by the…

A: An experiment known as a test-cross involves determining the genotype of an organism that is…

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.