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 carry either an X or a Y sex chromosome. If a sperm cell carries an X chromosome and fertilizes an egg with an X chromosome, the resulting embryo will be female. If a sperm cell carries a Y chromosome and fertilizes an egg with an X chromosome, the resulting embryo will be male.
Whether they have 2 X chromosomes= girl, of one X chromosome and one Y chromosome= boy
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.
An embryo with 2 X chromosomes develops into a female due to the presence of genes on the X chromosomes that promote the development of female reproductive structures and characteristics. These genes lead to the production of hormones that guide the development of female features during prenatal development.
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.