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during meiosis
Wolf-Hirschhorn syndrome is primarily caused by a deletion of a portion of chromosome 4, specifically at the 4p16.3 region. This chromosomal mutation is classified as a deletion mutation, where a segment of the chromosome is missing, leading to the loss of genetic material. The syndrome is characterized by developmental delays, distinctive facial features, and other congenital anomalies.
Galactosemia... the word "lactose" in this word should have given you a thoughtless answer.
Trisomy 13, also known as Patau syndrome, is a chromosomal mutation where there is an extra copy of chromosome 13 in each cell. This condition can lead to various physical and intellectual disabilities.
chromosomal mutation
Chromosomal mutation
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.
Nope, what you're thinking of is actually called an inversion mutation (a type of structural aberration); a chromosomal mutation is simply any sort of mutation that affects an organism's genotype.
a gene is passed on from generations and a chromosome is just found in certain cells
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gene mutation, chromosomal abberations
During meiosis
during meiosis
Yes
translocation
during meiosis