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Irina18 [472]
3 years ago
12

Match the atomic particles with their electrical charges.

Biology
1 answer:
Vinil7 [7]3 years ago
8 0
Proton is positive.(+)
Neutron is neutral(0)
Electron is negative(-)
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madreJ [45]

The pattern of inheritance of the offspring of a hemophiliac father would be heterozygous.

<h3>What is Hemophilia?</h3>

Hemophilia is defined as the sex–linked disorder that occurs due to an abnormality of the X chromosome.

A father that has hemophilia would be affected only on his X chromosome and can only pass it to their children making them carries.

This is because the children would inherit only one X chromosome from their father and a healthy X chromosome from their mother.

Learn more about chromosome here:

brainly.com/question/269366

#SPJ1

8 0
1 year ago
porque son los micronutrientes indispensables para los diferentes metabolicas de los organismos vivos?
Kipish [7]

Because they are the essential micronutrients for the different metabolites of living organisms?


8 0
3 years ago
The process of evolution is based on _____. phenotypic inheritance genotypic inheritance
Afina-wow [57]
The process of evolution is based on the genotypic inheritance as the genes changes overtime.
5 0
2 years ago
Read 2 more answers
Lesch-Nyhan syndrome is an X-linked, recessive condition caused by mutation of the HPRT1 gene responsible for purine metabolism.
Elanso [62]

Answer:

B. The father did not contribute a sex chromosome to his daughter due to nondisjunction of the sex chromosomes. The daughter is XO and her only X chromosome came from her mother, who was a carrier.

A.The mother's X chromosomes failed to separate during meiosis, and the daughter inherited two X chromosomes with the Lesch-Nyhan mutation. The father contributed no sex chromosomes.

Explanation:

As seen in the question above, a little girl was diagnosed with Lesch-Nyhan syndrome, which is an X-linked recessive condition caused by a mutation in the HPRT1 gene responsible for purine metabolism.

The little girl's parents do not have the syndrome, and no one in the little girl's paternal family presented this syndrome, however, we know that the maternal grandfather of the little girl's mother had the syndrome, which means that it was the mother's genetic material that contributed to the development of the syndrome in the little girl. This was because the little girl did not receive any X chromosomes from her father, but she inherited the two X chromosomes from her mother that coded for the Lesch-Nyhan mutation. This happened because the mother's X chromosome disjuction did not occur during meiosis I.

As shown above, the father did not contribute any sex chromosomes to his daughter, which means that the daughter is XO and her only X chromosome came from her mother, who was a carrier.

3 0
2 years ago
If Rochester were a cell, what would be the nucleus?
Natasha_Volkova [10]

Answer:

correct answer is A

Explanation:

nucleus is most important part of a cell as a town hall would be to a city

7 0
2 years ago
Read 2 more answers
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