They are typed as telocentric acrocentric
nucleus → chromosome → gene
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There are 3 types of Turner syndrome Classic Turner syndrome - 45X - second X chromosome missing from all cells. Mosaic Turner syndrome - 45X/46XX - second X chromosome missing from some cells. The third type of Turner syndrome is when the second X chromosome is damaged or only partly missing.
The parts of a chromosome that control inherited traits is referred to as genes. There are many types of inherited traits, some visible while the others are invisible,
Deletion, duplication, inversion, translocation.
autosomal dna, X chromosome, Y chromosome,and mitochondrial
nucleus → chromosome → gene
The four types of chromosomal mutation are deletion, duplication, inversion and trasnlocation. Deletion is the loss of all or part of a chromosome. Duplication is where a segment of a chromosome is copied. Inversion is where a section of a chromosome is reversed. Translocation is the process in where a part of one chromosome breaks off and attaches to a non-homologous chromosome.
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A deletion mutation can take genes away from a chromosome.
Four types of chromosomal mutations are Down syndrome (which is a mutation in which there are three copies of chromosome 21), Kinefelter Syndrome (which is a mutation in which a male has an extra X-chromosome), Turner Syndrome (which is a mutation in which a female is missing an X-chromosome), and Patau Syndrome (which is a mutation in which there are three copies of chromosome 13).
The four types of alterations of chromosome structure are deletion, duplication, inversion, and reciprocal translocation. Deletion is the loss of one or more nucleotides from a gene by mutation; the loss of a fragment of a chromosome. Duplication is repition of a part of a chromosome resulting from fusion with a fragment froma homologous chromosome. Duplication can result from an error in meiosis or from mutagenesis. Inversion is a change in a chromosomeresulting from reattachment of a chromosome fragment to the original chromosome, but in a reverse direction. Mutagens and errors during mesosis can cause inversions. Translocation is the attachment of a chromosomal fragment to a nonhomologous chromosome.
There are two kinds of sex chromosome X and Y that result in two different sex types: XX in females and XY in males. A child will always get a X chromosome from their mother, but the sex depends on which chromosome the male gives, which is completely random, you could get the X chromosome making you female or you could get the Y chromosome making you male.
Four types of chromosomal mutations are Down syndrome (which is a mutation in which there are three copies of chromosome 21), Kinefelter Syndrome (which is a mutation in which a male has an extra X-chromosome), Turner Syndrome (which is a mutation in which a female is missing an X-chromosome), and Patau Syndrome (which is a mutation in which there are three copies of chromosome 13).
There are 3 types of Turner syndrome Classic Turner syndrome - 45X - second X chromosome missing from all cells. Mosaic Turner syndrome - 45X/46XX - second X chromosome missing from some cells. The third type of Turner syndrome is when the second X chromosome is damaged or only partly missing.
The parts of a chromosome that control inherited traits is referred to as genes. There are many types of inherited traits, some visible while the others are invisible,
Deletion, duplication, inversion, translocation.