Autosomal aneuploidy is usually lethal due to genetic_________

Q: O Autosomal Dominant

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Q: ll me whether it is autosomal reccessive inheritance,autosomal domiant inheritance,sex-linked…

A: Inheritance modes are a type of inheritance. Mutations in the parents' DNA are passed on to the…

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: A woman with type O blood gave birth to a baby, also with type O blood. The woman stated that a man…

A: Human genetics clearly explain blood groups. In order to understand a baby's blood group with O and…

Q: A homozygous dominant

A: In genetics, dominance refers to the phenomenon of one gene variant on one chromosome masking or…

Q: Mary has type O blood type . Frank has homozygous type B blood type. Mary had a child with type O…

A: Mary genotype is OO while the male has genotype BB so when we cross these we get BO,BO,BO,BO blood…

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: What type of inheritance is shown in the pedigree? II II sex linked recessive autosomal recessive…

A:

Q: The pedigree shown is A) Autosomal Dominant B) Autosomal Recessive C) Sex linked D) Sex linked…

A: In the given pedigree, the trait skips generation i.e., two unaffected parents have affected…

Q: Understanding x - linked dominant/ recessive inheritance patters

A: X-linked inheritance is specifically a sex linked inheritance where the trait inheritance within the…

Q: To determine: The possible reason for identical twins not having similar and not identical…

A: DNA fingerprinting is a technique for determining the nucleotide sequences of specific areas of…

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: The genotype XO corresponds to:

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

Q: male having genotype AaBbCC mates with a female having genotype aaBBcc.

A: The fork line method can be used by figuring the occurrence of each gene or set of genes to be found…

Q: The possible genotype and phenotype of parents of a girl who has blood group O.

A: Genetics may be a branch of biological sciences that studies genes, genetic variation, and heredity…

Q: Mention any two autosomal genetic disorders with their symptoms.

A: Introduction The two autosomal genetic disorders with their symptoms are as follows.

Q: The gene that determines whether a child becomes a Male or a female is located on a specific pair of…

A: There are two types of chromosomes found in our body, autosomes and allosomes.  Autosomes are found…

Q: B A In the image above, the tissue found at letter B is; Нaploid Diploid Neither

A: The above image belongs to the ferns. It is the prothallus of the fern developed from spores.

Q: A person known to be born with one X-chromosome, zero or no known Y chromosome, trisomy 21, and…

A: Introduction  Most of the organisms present on earth are diploid which means they contain two sets…

Q: What is autosomal

A: Autosomes are those chromosomes that are not sex chromosomes, humans have 22 pairs of autosomes and…

Q: tables attached to complete the punnett square   Eye color Parental genotypes: ______ X ______…

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

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: Sex: Chromosomal anomaly: Syndrome:

A: The sex of the given karyotype is Male . As there are X and Y chromosomes.

Q: Assuming sexual reproduction and that no mutations have occurred. Please draw one possible genotype…

A: Genotype It is a description of our DNA's pair of alleles. The genotype of an offspring is…

Q: Homologous pairs of chromosomes carry genes controlling the same inherited traits. True False

A: Homologous chromosomes are similar in shape, size and length. Their centromere position is same.

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

A: Answer: AUTOSOMAL DOMINANT : It is the disorder where the either of the allele is dominant…

Q: Interpreting the karyotype Lab technicians compile karyotypes and then use a specific notation to…

A: Karyotyping refers to the photographic arrangement of the complete set of individual's chromosome in…

Q: A female who is a carrier for an autosomal recessive disorder has the genotype

A: (Please note that, you have submitted two question, we can only answer to one question at a time,…

Q: A patient has two parents with Huntington's disease. They may not have inherited this autosomal…

A: The Huntington's disease is a very rare condition and is an inherited disease which results in…

Q: This question is about a medical condition that is inherited as an autosomal dominant allele. In…

A: Autosomal dominant diseases effect a person even when in heterozygous state but sometimes their…

Q: difference of ideogram and karyotype

A:

Q: sa sex-linked, recessive disorder (X). Using the details below, fill in the Punnett square to…

A:

Q: Tell me whether it is autosomal reccessive inheritance,autosomal domiant inheritance,sex-linked…

A: Pedigree analysis helps us determine the pattern of inheritance of a trait. In this case the trait…

Q: Incomplete dominance And must show the Punnet square

A:

Q: My Diagnosis for Pati Sex: Chromosomal Disorder Justification:

A: Chromosomes are the parts of your cells that contain your genes. Genes are parts of DNA passed down…

Q: ĮBIB or IBi = B dom/rec 3. A man with type A blood marries a woman with type B blood. Their child…

A: Blood group is controlled by three alleles IA, IB, i alleles. It is the case of multiple allelism.

Q: Dominant vs. Recessive genes

A: The fundamental physical and functional unit of heredity is the gene.

Q: A child has sex-linked color blindness, however both parents have normal color vision Please…

A: Color blindness is the X-linked recessive disorder that means it is inherited X-chromosomally and…

Q: how An inversion can affect phenotype

A: Mutation is the sudden heritable changes that occur in the DNA sequences due to error while copying…

Q: Red/green colorblindness X-recessive pedigree

A: Answer: X-linked recessive pedigree is a pedigree chart of a family in which the disease is transfer…

Q: If two parents are heterozygous for an autosomal recessive disease, they are both considered genetic…

A: A gene, disorder, or disease may be passed down across families in a number of ways, including…

Q: detacched earlobe phenotype and genotypes

A: A genotype is the genetic makeup of an organism. Phenotype is the observable morphological…

Q: The genotype AABBCcDD will have the following gametes

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Q: Gilbert's genetic makeup is homozygous for dark hair. Jan's is homozygous for blond hair. What…

A: Gilbert has genetically dark hair colour. Jan has genetically blond hair colour. Both of them have…

Q: Chromosomal Abnormalities Classification of abnormality Name of Number of Description Affected…

A: Hello, as you have posted question with multiple sub-parts, we will answer the first three…

Q: Janavi and Mehmet are the parents in this family: all others on the gel are children. Son Ravi is…

A: Ravi is born with the blood disorder as it can be observed from the figure that Ravi has acquired B…

Q: Name of Disorder Dom. or Recessive Autosomal or Sex Linked Type of Mutation Phenotype Cystic…

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

Q: Using the karyotype and the disorder charts below, which of the following abnormalities is true for…

A: Karyotype:- Karyotyping is the process of matching and ordering all of an organism's chromosomes,…

Q: Blue eyes Brown eyes Heterozygous Homozygous BB Bb bb O O O

A: Human cells carry two copies of each chromosomes and they have two versions of each gene. An allele…

Mitochondrial Mutations

A mitochondrion is a cellular organelle that serves as the site for cellular respiration and energy production (ATP or Adenosine Triphosphate). It is a double-membrane-bound organelle and is only present in eukaryotic cells.