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What else can I help you with?
What cause fragile X syndrome?
The fragile X syndrome is a genetic disorder caused by mutation of the FMR1 gene on the X chromosome.
What is osteroporosis?
Condition caused by calcium deficiency; bones become porous, weak, and fragile.
What were the two main problems caused by using valves in colossus?
Reliability and heat were the main problems. Valves were fragile devices that, due to the relatively primitive way they were manufactured, failed pretty quickly. In addition to that, they gave off vast amounts of heat. This meant they needed expensive air-conditioning systems to keep their temperature down.
What is an example of a genetic disorder that is caused by insertion of extra codons in the X sex chromosome?
Fragile X Syndrome
What is an example of a genetic disorder that is caused by insertion of extra codons in x sex chromosome?
Fragile X Syndrome
What is an example of a genetic disorder that is caused by insertion of extra codons of the X sex chromosome?
Fragile X Syndrome
What is an example of a genetic disorder that is caused by insertion of an extra codons in the X sex chromosome?
Fragile X Syndrome
What disease is caused by insertion mutation?
For example, some diseases caused by insertional mutations include: Fragile X Syndrome. Huntington's Disease. Myotonic dystrophy. Cystic fibrosis.
Does fragile x syndrom have a mutation?
Yes, fragile X syndrome is caused by a mutation in the FMR1 gene on the X chromosome. This mutation leads to a lack of production of a protein called FMRP, which is essential for normal brain development.
How do you put fragility in a sentence?
The vase's fragility caused it to break when i picked it up. -tippytoes1998
The pressure and heat that produces magma are caused in part by?
Radioactive elements
How many chromosome do you have when you have fragile x syndrome?
Fragile X syndrome is caused by a mutation that prevents the Fragile X mental retardation (Fmr-1) gene from being transcribed. This gene is located on the X chromosome (the sex chromosome). Since males only carry one of these chromosomes, they are twice as likely to be affected by the mutation than females.
