Turner syndrome is a disease in which an individual is born with only a single X chromosome. Suppose the woman in the couple is a carrier for hemophilia and has a child with Turner syndrome. Would this child have the disease?

Q: In Drosophila melanogaster, white eyes (w) is an X-linked recessive mutation. Normal eyes are red…

A: The normal eyes are red in Drosophila melanogaster. Normal red eyes are represented by W. Whereas,…

Q: What disorder is shown in the following karyotype? Explain your reasoning and describe any other…

A: The above image is a karyotype of a person. Karyotypes depict paired and ordered chromosomes and are…

Q: All of the following would be visible on a karyotype except O aneuploidy. polysomy. trisomy.…

A: A karyotype is a person's assortment of chromosomes. The term additionally alludes to a research…

Q: A man with a specific unusual genetic trait marries an unaffected woman. For each type of…

A: Pedigree is a family chart showing the inheritance of a particular trait through several generation…

Q: Please write in digital format Define the following terms: a) Triploid b) Monosomic c) Trisomic d)…

A: Normal cell has a diploid number of chromosomes. Each cell has 23 pairs of chromosomes out of which…

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

A:

Q: Male pattern baldness is inherited on the X chromosome. The allele for baldness is designated Xb,…

A: Baldness refers to the complete loss of hairs that leads to a visible scalp. If hair loss gets…

Q: The following pedigree shows a pattern of inheritance that is found in which of the following…

A:

Q: The above pedigree represents the inheritance of a disease that is most likely Autosomal Dominant…

A: Pedigree is defined as the diagrammatic representation of family members for a particular trait.

Q: a) A woman who is type A has a daughter who is type O. Give the genotypes of both the mother and of…

A: The human blood group or ABO blood group system is an example of codominant alleles. There are three…

Q: The genotype XO corresponds to:

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

Q: Imagine that you are a genetic counselor, and a couple planning to start a family comes to you for…

A: During gamete formation, two alleles of a gene segregate into different gametes. This is based on…

Q: During the pathoanatomic inspection of a baby-boy's dead body the following abnormalities:…

A: Chromosomal disorder are the abnormalities that arises due to alterations in chromosome arrangement…

Q: individual male or female? How do you know? Was there anything unusual about your Karyotype?…

A: Human sex is mainly two types, male and female. Identification based on in general through…

Q: Using the pedigree, assume th

A: The pedigree chart is a diagram, which displays the appearance of the phenotypes of a particular…

Q: A B C genotype locus phenotype

A: Gene The gene is the unit of genetic information that controls a specific aspect of the phenotype.…

Q: The autosomal (not X-linked) gene for brachydactyly, short fingers, is dominant to normal finger…

A: Given: The autosomal (not X-linked) gene for brachydactyly, short fingers, is dominant to normal…

Q: The pedigree shows inheritance of an autosomal recessive disease in an extended family. Assume…

A: Although the trait is skipped in the pedigree, autosomal recessive inheritance is discovered. The…

Q: Is this pedigree dominant or recessive? Autosomal or sex-linked? What is also usual about this…

A: The pedigree is the genetical analysis that gives us idea about the inheritance pattern of a…

Q: Ann's family has a history of cystic fibrosis, a recessive genetic disease. In the pedigree, family…

A: A pedigree chart is a diagram that shows the occurrence and appearance of phenotypes of a particular…

Q: From this pedigree is it dominant or recessive. Is ur autosomal or sex-linked?

A: Pedigree is define a diagrammatic representation of the individuals of a family for a particular…

Q: Classical hemophilia is a sex-linked disease caused by a recessive gene on the X chromosome.…

A: Hemophilia is a X linked recessive trait.  Let X allele encodes normal phenotype. And it is dominant…

Q: I II II A

A: The genes located on the nuclear chromosomes obey the Mendelian law of inheritance. In the human…

Q: Greg and Susan have Nail-Patella syndrome. Greg has A blood in ci inherited from his mother. Susan…

A: In this question linkage is observed where two genes are linked together because they are placed at…

Q: Is this pedigree autosomal dominant, autosomal recessive, or X-linked recressive? Can you please…

A: Autosomal dominant and Autosomal recessive: The word autosomal refers to the "autosomes" which means…

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: Recessive hemophilia, x-linked. The man has it, and his wife is a carrier. Draw a Punnett square to…

A: Parent 1 Male  - Hemophilia (Xh Y) Parent 2 Female – Carrier (Xh X) In the above cross, XhXh…

Q: Kelly and Sam are both unaffected carriers for two autosomal recessive disorders, PKU (chromosome…

A: Sir Gregor Mendel was a priest and a teacher who did the famous hybridization experiment on garden…

Q: Ali and Ayşe have a sibling with PKU (a recessive disorder). Neither Ali nor Ayşe nor any of their…

A: Phenylketonuria (PKU) is an autosomal recessive inherited disorder of metabolism which results in…

Q: A man and a woman do not have hemophilioa, but the womans father did. (Hemophilia is X-linked…

A: (Note: According to the given guidelines, we are supposed to answer only one question. Please repost…

Q: An individual comes into your genetics clinic to be tested for any anomalies. When looking at their…

A: Given: An individual come to your genetics clinic to be tested for any anomalies.When looking at…

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: Duchenne muscular dystrophy is a recessive disorder caused by a rare,loss-of-function allele that is…

A: Duchenne muscular dystrophy (DMD) is a quickly progressive type of muscular dystrophy that happens…

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: In Drosophila melanogaster, white eyes (w) is an X-linked recessive mutation. Normal eyes are red…

A: Inheritance is defined as the passing of genetic inheritance from parental to next generation.

Q: Given the karyogram below, anSW Is this a male or female? female Do you see any abnormality? Yes 13…

A: Karyotyping is the procedure by which photos of chromosomes are taken so as to decide the chromosome…

Q: The pedigree below shows the occurrence of Becker muscular dystrophy in a family. Becker muscular…

A: The mode of inheritance is a pattern of obtaining parentral alleles  or genes to the offsprings. The…

Q: Duchenne muscular dystrophy is a sex-linked recessive disorder characterized by a progressive loss…

A: DNA is the genetic material in most living organisms. It is the information hub of the cell that…

Q: The pedigree shows inheritance of an autosomal recessive disease in an extended family. Assume…

A: Autosomal recessive inheritance is found because the trait is skipped in the given pedigree.  Let A…

Q: A man with a specific unusual genetic trait marries an unaffected woman. For each type of…

A: Pedigree chart is a illustrative represented showing family members of various generation . With…

Q: Single nucleotide polymorphisms do not show mendelian segregation through meiosis. Is this true or…

A: Non-Mendelian inheritance is a pattern of inheritance in which the traits governed by alleles do not…

Q: Draw two replicated, condensed, homologous chromosomes that have the genes E and F on them. This…

A: Morgan's Theory --Thomas Hunt Morgan (Father of modern and experimental genetics ) ,discovered the…

Q: The pedigree of a family with haemophilia as shown in Figure below .  If the gene for haemophilia is…

A: Pedigree is a chart prepared from.symbols and lines which are used to represent genetic family…

Q: In the karyotype shown here, identify the sex chromosomes. Is this individual a male or a female?

A: Introduction Any cell contains a specific number of chromosomes referred to as ploidy level or…

Q: Galactosemia is a recessive human disease that istreatable by restricting lactose and glucose in the…

A: Gene: Genes are genetic material that passes from parents to progeny. The dominant allele can…

Q: The following pedigree describes the inheritance of Lesch-Nyhan syndrome, an X-linked recessive…

A: Lesch-Nyhan syndrome is a disorder that affects virtually entirely men. It is distinguished by…

Q: 3 10 12 %3D 13 14 15 16 17 18 38 19 20 21 22

A: Karyogram - It is a photograph containing chromosomes of an organism in which it's   arranged by…

Q: An individual has the genotype AabbCC.  The A gene is located on chromosome 1 while the B and C…

A: For an individual with a genotype AabbCC. The gene A present on chromosome 1 is heterozygous with…

Q: The ABO blood type locus has been mapped on chromosome 9. A father with blood genotype BO blood and…

A: The presence or absence of the antigens A and B, which are borne on the surface of red blood cells,…

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

A: As per Bartleby's answering policy, we can answer only one question with a maximum of three…

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.