Individuals with to matchin X chromosomes are female. So, XX Is the chromosomal configuration that denotes female :)
The electron configuration of potassium (K), which has an atomic number of 19, in long form is 1s² 2s² 2p⁶ 3s¹. In short form, it can be represented as [Ar] 4s¹, where [Ar] denotes the electron configuration of argon, the nearest noble gas preceding potassium.
The electron configuration of magnesium in long form is 1s² 2s² 2p⁶ 3s². In short form, it can be represented as [Ne] 3s², where [Ne] denotes the electron configuration of neon, which accounts for the filled inner shells. Magnesium has a total of 12 electrons, and the configuration reflects its position in group 2 of the periodic table.
well I am a teacher and I say that it is elements and compounds
Hyenas have a diploid chromosome number of 38. This means that in their somatic cells, they contain 38 chromosomes arranged in 19 pairs. This chromosomal configuration is typical for members of the family Hyaenidae.
Deletion: loss of a chromosomal segment. Duplication: repetition of a chromosomal segment. Inversion: reversal of a chromosomal segment. Translocation: movement of a chromosomal segment to a new location on a different chromosome.
The gene present on the sex chromosome either in recessive or dormant condition is called a sex linked gene. For example gene for color blindness present on X chrosome. It is carried by a female and mostly affect the male because male have XY type of chromosomal configuration.
The gene present on the sex chromosome either in recessive or dormant condition is called a sex linked gene. For example gene for color blindness present on X chrosome. It is carried by a female and mostly affect the male because male have XY type of chromosomal configuration.
46, XY
46, XY
Chromosomal Loci is a Heterozygous
No, the chromosomal difference between cattle and humans would prevent a human female from conceiving a fetus with a bovine male.
Females are much less likely to suffer from hemophilia because it is a recessive X linked genetic disorder. Women, having the chromosomal configuration of XX would need both X chromosomes to carry the marker for hemophilia because it is a recessive gene. Whereas men, with the chromosomal configuration of Xy do not have a "backup" X chromosome so if their only X chromosome has the hemophiliac trait, then that man will be a hemophiliac.
The electron configuration of potassium (K), which has an atomic number of 19, in long form is 1s² 2s² 2p⁶ 3s¹. In short form, it can be represented as [Ar] 4s¹, where [Ar] denotes the electron configuration of argon, the nearest noble gas preceding potassium.
The electron configuration of magnesium in long form is 1s² 2s² 2p⁶ 3s². In short form, it can be represented as [Ne] 3s², where [Ne] denotes the electron configuration of neon, which accounts for the filled inner shells. Magnesium has a total of 12 electrons, and the configuration reflects its position in group 2 of the periodic table.
There is no actual chromosomal change, there is an extra chromosome.
Chromosomal mutation can have lasting impacts on the person who this happens to. A version of a chromosomal mutation is the mutation that leads to Down's Syndrome.
1s2 2s2 2p6 3s2 3p6 4s2 3d3