XO
The question is not really clear. A karyotype is the overall complement of chromosomes isolated from a cell or organism (eukaryotic). When the karyotype of a normal healthy female is prepared for viewing by a cytogeneticist, there are 22 pairs of autosomal chromosomes present (ie two of chromosome 1, two of chromosome 2 etc...). There is one additional pair of sex chromosomes (two copies of X). A normal healthy human male also has 22 pairs of autosomes but the pair of sex chromosomes is not matched but instead there is one X chromosome and one Y chromosome (which is smaller than the X). So, if you look at a karyotype that has been laid out - if the two sex chromosomes are different sizes (X and Y) then the karyotype is from a male, if however they are the same size (X and X) then the karyotype is from a female.
It results in a female:) im pretty sure you go to primavera like me, biology is tough isn't it?
The chart used to determine a person's sex is called a karyotype chart. This chart displays the chromosomes found in an individual's cells, which can help determine their biological sex based on the presence of XX (female) or XY (male) chromosomes.
Chromosomal disjunction during meiosis leaving one of the gametes that meet in random fertilization short an X chromosome is the simplest fertilization mishap that results in Turner's syndrome. One X chromosome.
a biologically male individual. The XY genotype typically refers to the genetic makeup of males in humans, where X represents one of the sex chromosomes inherited from the mother and Y represents the sex chromosome inherited from the father.
A male grasshopper has two different sex chromosomes, XY, while a female grasshopper has two of the same sex chromosomes, XX. This difference in sex chromosome composition determines the sex of the grasshopper.
The sex of an individual can be determined by analyzing the karyotype for the presence of sex chromosomes. A karyotype with two X chromosomes is typically female (XX), while a karyotype with one X and one Y chromosome is typically male (XY). This distinction is made based on the presence or absence of the Y chromosome, which carries genes related to male development.
The question is not really clear. A karyotype is the overall complement of chromosomes isolated from a cell or organism (eukaryotic). When the karyotype of a normal healthy female is prepared for viewing by a cytogeneticist, there are 22 pairs of autosomal chromosomes present (ie two of chromosome 1, two of chromosome 2 etc...). There is one additional pair of sex chromosomes (two copies of X). A normal healthy human male also has 22 pairs of autosomes but the pair of sex chromosomes is not matched but instead there is one X chromosome and one Y chromosome (which is smaller than the X). So, if you look at a karyotype that has been laid out - if the two sex chromosomes are different sizes (X and Y) then the karyotype is from a male, if however they are the same size (X and X) then the karyotype is from a female.
A super female, also known as a 47,XXX female, has an atypical karyotype characterized by the presence of an extra X chromosome, resulting in a total of three X chromosomes instead of the typical two. This condition can lead to a range of developmental and physical features, although many individuals may be asymptomatic and lead normal lives. The extra chromosome is usually a result of nondisjunction during meiosis. Super females may have a slightly increased risk of learning disabilities and other health issues, but many are unaffected.
Turner syndrome is characterized by a karyotype with 45 chromosomes, including a single X chromosome (X0). This syndrome is associated with short stature, webbed neck, and infertility in individuals with female characteristics.
It results in a female:) im pretty sure you go to primavera like me, biology is tough isn't it?
In humans and most (if not all) other eukaryote species, males have the karyotype XY in their chromosomes, and females have the genotype XX.
In the ZW sex chromosome system, the male genotype is ZZ. The letter Z represents the presence of a dominant male-determining gene, while the letter W represents the absence of this gene, which determines female development. Therefore, individuals with the ZZ genotype develop as males in this system.
The karyotype notation 45,XX,-5 indicates a female individual with 45 chromosomes, including two X chromosomes. The "-5" suggests the loss of one copy of chromosome 5. This type of karyotype abnormality can be associated with certain genetic disorders or diseases.
Individuals with color blindness often have a normal male karyotype (46,XY) or female karyotype (46,XX). The genetic basis for color blindness typically involves mutations in genes located on the X chromosome, leading to different types of color vision deficiencies.
XXY-Klinefelter syndromePeople with Klinefelter syndrome are also tall male phenotype. They are sterile, may show mild mental impairment, and may develop enlarged breast because of the extra X chromosome.
To be female, an individual must inherit two X chromosomes, one from each parent. This means that a female has the genotype XX. In contrast, males typically have one X and one Y chromosome (XY). Thus, the presence of two X chromosomes is what determines female sex in humans.