<span>The vibrations are then sent to three tiny bones in the middle ear: the malleus, incus, and stapes. These bones then amplify the sound vibrations and send them to the cochlea, a snail-shaped structure in the inner ear. The vibrations then cause the fluid inside the cochlea to ripple along the basilar membrane. This ripple stimulates the hair cells that sit on top of the basilar membrane.</span>
Answer:
recessive gene
Explanation:
mainly masked by thee dominant gene eg Tt where T is dominant over t,,,there t is recessive..
Answer:
....
i dont know i just want points...
Explanation:
im sorry...i just wanted my aplogizes
The Prader-Willi syndrome (PWS) is due to the lack of expression of paternal genes of the 15q11-q13 region. It usually occurs sporadically, although some family cases have been described (<1%). Approximately 70% of cases are produced by deletions of paternal origin in the 15q11-q13 region. 28% of cases are due to maternal uniparental disomy and less than 2% are caused by imprinting alterations. A geneticist studying prader-willi syndrome should focus on chromosome 15, its structure or changes in the number, these anomalies are also related to other syndromes such as: Bloom Syndrome, Breast cancer, Isovaleric acidity among others.
Answer:
d: store minerals, like calcium
Explanation:
i'm really sorry if i'm wrong,but if it is correct then i'm glad i could help :)
