Home » Without Label » Can A Recessive Trait Be On The Y Chromosome - Can A Recessive Trait Be On The Y Chromosome : Brainteaser ... : This is a pleiotropic trait.
Can A Recessive Trait Be On The Y Chromosome - Can A Recessive Trait Be On The Y Chromosome : Brainteaser ... : This is a pleiotropic trait.
Can A Recessive Trait Be On The Y Chromosome - Can A Recessive Trait Be On The Y Chromosome : Brainteaser ... : This is a pleiotropic trait.. An individual with these traits is an albino. since the gene for albinism is recessive, it only shows up in the phenotype of homozygous recessive people. The x chromosome will contain the alleles for the trait and the y chromosome will have no alleles for this trait. (for more information on this disorder, choose "c syndrome" as your search term in the rare disease database.) many other chromosomal disorders have features similar to chromosome 13, partial monosomy 13q. C syndrome is thought to be inherited as an autosomal recessive genetic trait. This is a pleiotropic trait.
C syndrome is thought to be inherited as an autosomal recessive genetic trait. The x chromosome will contain the alleles for the trait and the y chromosome will have no alleles for this trait. This is a pleiotropic trait. An individual with these traits is an albino. since the gene for albinism is recessive, it only shows up in the phenotype of homozygous recessive people. The genetically inherited condition in which there is a marked deficiency of pigmentation in skin, hair, and eyes.
The genetically inherited condition in which there is a marked deficiency of pigmentation in skin, hair, and eyes. C syndrome is thought to be inherited as an autosomal recessive genetic trait. (for more information on this disorder, choose "c syndrome" as your search term in the rare disease database.) many other chromosomal disorders have features similar to chromosome 13, partial monosomy 13q. This is a pleiotropic trait. The x chromosome will contain the alleles for the trait and the y chromosome will have no alleles for this trait. An individual with these traits is an albino. since the gene for albinism is recessive, it only shows up in the phenotype of homozygous recessive people.
An individual with these traits is an albino. since the gene for albinism is recessive, it only shows up in the phenotype of homozygous recessive people.
The x chromosome will contain the alleles for the trait and the y chromosome will have no alleles for this trait. C syndrome is thought to be inherited as an autosomal recessive genetic trait. This is a pleiotropic trait. An individual with these traits is an albino. since the gene for albinism is recessive, it only shows up in the phenotype of homozygous recessive people. The genetically inherited condition in which there is a marked deficiency of pigmentation in skin, hair, and eyes. (for more information on this disorder, choose "c syndrome" as your search term in the rare disease database.) many other chromosomal disorders have features similar to chromosome 13, partial monosomy 13q.
This is a pleiotropic trait. The x chromosome will contain the alleles for the trait and the y chromosome will have no alleles for this trait. The genetically inherited condition in which there is a marked deficiency of pigmentation in skin, hair, and eyes. (for more information on this disorder, choose "c syndrome" as your search term in the rare disease database.) many other chromosomal disorders have features similar to chromosome 13, partial monosomy 13q. C syndrome is thought to be inherited as an autosomal recessive genetic trait.
This is a pleiotropic trait. (for more information on this disorder, choose "c syndrome" as your search term in the rare disease database.) many other chromosomal disorders have features similar to chromosome 13, partial monosomy 13q. The x chromosome will contain the alleles for the trait and the y chromosome will have no alleles for this trait. The genetically inherited condition in which there is a marked deficiency of pigmentation in skin, hair, and eyes. C syndrome is thought to be inherited as an autosomal recessive genetic trait. An individual with these traits is an albino. since the gene for albinism is recessive, it only shows up in the phenotype of homozygous recessive people.
The x chromosome will contain the alleles for the trait and the y chromosome will have no alleles for this trait.
The x chromosome will contain the alleles for the trait and the y chromosome will have no alleles for this trait. An individual with these traits is an albino. since the gene for albinism is recessive, it only shows up in the phenotype of homozygous recessive people. This is a pleiotropic trait. C syndrome is thought to be inherited as an autosomal recessive genetic trait. The genetically inherited condition in which there is a marked deficiency of pigmentation in skin, hair, and eyes. (for more information on this disorder, choose "c syndrome" as your search term in the rare disease database.) many other chromosomal disorders have features similar to chromosome 13, partial monosomy 13q.
C syndrome is thought to be inherited as an autosomal recessive genetic trait. The genetically inherited condition in which there is a marked deficiency of pigmentation in skin, hair, and eyes. (for more information on this disorder, choose "c syndrome" as your search term in the rare disease database.) many other chromosomal disorders have features similar to chromosome 13, partial monosomy 13q. An individual with these traits is an albino. since the gene for albinism is recessive, it only shows up in the phenotype of homozygous recessive people. The x chromosome will contain the alleles for the trait and the y chromosome will have no alleles for this trait.
(for more information on this disorder, choose "c syndrome" as your search term in the rare disease database.) many other chromosomal disorders have features similar to chromosome 13, partial monosomy 13q. This is a pleiotropic trait. C syndrome is thought to be inherited as an autosomal recessive genetic trait. The x chromosome will contain the alleles for the trait and the y chromosome will have no alleles for this trait. The genetically inherited condition in which there is a marked deficiency of pigmentation in skin, hair, and eyes. An individual with these traits is an albino. since the gene for albinism is recessive, it only shows up in the phenotype of homozygous recessive people.
An individual with these traits is an albino. since the gene for albinism is recessive, it only shows up in the phenotype of homozygous recessive people.
This is a pleiotropic trait. The genetically inherited condition in which there is a marked deficiency of pigmentation in skin, hair, and eyes. The x chromosome will contain the alleles for the trait and the y chromosome will have no alleles for this trait. C syndrome is thought to be inherited as an autosomal recessive genetic trait. An individual with these traits is an albino. since the gene for albinism is recessive, it only shows up in the phenotype of homozygous recessive people. (for more information on this disorder, choose "c syndrome" as your search term in the rare disease database.) many other chromosomal disorders have features similar to chromosome 13, partial monosomy 13q.