Yes, an embryo can develop with one X chromosome, rather than the XX or XY chromosome pair. An example of this is girls born with Turner's syndrome, who have only one X chromosome.
The X and Y sex chromosomes. If the embryo inherits an X and Y chromosome, it will be male. If the embryo inherits two X chromosomes, it will be female.
An embryo, male or female, usually has two sex chromosomes, one from mom, one from dad. In a male's case, they would be XY. Rarely, nondisjunction occurs, and a child winds up XXX, XXY, XYY, or X. XXX and X become female, and XXY and XYY become male. So, it is theoretically possible for a male embryo to have three sex chromosomes.
A sperm cell contains either an X or Y sex chromosome, determining the biological sex of the offspring when combined with an egg. This ensures that the resulting embryo will have the proper number of sex chromosomes (XX for female or XY for male) to develop into a healthy individual.
Whether they have 2 X chromosomes= girl, of one X chromosome and one Y chromosome= boy
It is a male.
The sex of an embryo is determined by the presence or absence of a Y chromosome. If the embryo has a Y chromosome, it will develop as male. If no Y chromosome is present, the embryo will develop as female.
The X and Y sex chromosomes. If the embryo inherits an X and Y chromosome, it will be male. If the embryo inherits two X chromosomes, it will be female.
The sex of an embryo is determined by the combination of sex chromosomes inherited from the mother and father. Typically, females have two X chromosomes (XX) and males have one X and one Y chromosome (XY). The presence of a Y chromosome triggers the development of male characteristics.
It probably has to do with the predetermination of the baby's sex. If the father contributed a Y chromosome, then the indifferent gonads would develop into testes. If an X was contributed then they would develop into ovaries.
An embryo, male or female, usually has two sex chromosomes, one from mom, one from dad. In a male's case, they would be XY. Rarely, nondisjunction occurs, and a child winds up XXX, XXY, XYY, or X. XXX and X become female, and XXY and XYY become male. So, it is theoretically possible for a male embryo to have three sex chromosomes.
A sperm cell contains either an X or Y sex chromosome, determining the biological sex of the offspring when combined with an egg. This ensures that the resulting embryo will have the proper number of sex chromosomes (XX for female or XY for male) to develop into a healthy individual.
One X chromosome and one Y chromosome, which determines male sex characteristics.
Sperm cells are of two types. One type carries a Y chromosome, while the other type carries an X chromosome. This is the reason why the Spermatid is the 'deciding factor' in whether a baby will be male or female. The Ovum always carries an X chromosome.
Lesch-Nyhan syndrome is an X-linked recessive disorder, meaning the gene mutation responsible for the condition is located on the X chromosome. Males have one X chromosome and one Y chromosome, so if they inherit the mutated gene on their X chromosome, they will develop the disorder. Females have two X chromosomes, so they are less likely to inherit the mutation on both X chromosomes.
Whether they have 2 X chromosomes= girl, of one X chromosome and one Y chromosome= boy
Most sex-linked traits are found on the X chromosome because males have only one X chromosome, so any gene on the X chromosome will be expressed in males. In females, who have two X chromosomes, one X chromosome can compensate for any harmful gene on the other X chromosome.
In humans, typically a combination of one X chromosome from the mother and one X or one Y chromosome from the father determines the biological sex of the offspring. A fetus with XX chromosomes typically develops as female, while those with XY chromosomes develop as male.