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KATRIN_1 [288]
3 years ago
5

Hemophilia is an X-linked recessive disorder that is passed through generations and can be traced by using a pedigree.

Biology
1 answer:
GREYUIT [131]3 years ago
5 0

The half colored half white circle indicates that the person is a carrier but doesn't have the disease. Since John has a capital H we can assume that if someone else has a capital H genotype then they don't have it. Every body but Fred and Luke have a capital H and their squares are fully colored meaning that they have hemophilia

The answer is Fred and Luke

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Hey there!

I'm assuming it's pointing to the wall in between the two sections of the heart.

We can go over the function of the blue section and red section of the heart. Though I must admit I am not well versed with hearts of birds, I will assume this is similar to a human one. The blue section <u>receives blood from the body which doesn't have any oxygen left in it,</u> and the red section <u>receives blood from the lungs, newly oxygenated.</u> This sector in between separates these two sections, and separates oxygen-poor blood and oxygen-rich blood.

Thus, your answer is option D.

Hope this helps, feel free to let me know if you have any additional questions about this specific problem!

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3 years ago
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nikdorinn [45]

Answer:

In the first stage of sexual reproduction, "meiosis", the number of chromosomes is reduced from a diploid number (2n) to a haploid number (n). During "fertilisation", haploid gametes come together to form a diploid zygote, and the original number of chromosomes is rest

Explanation:

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Xelga [282]

Answer:

The correct answer would be - medium with lactose present and glucose absent.

Explanation:

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In the absence of glucose and lactose is present, due to inducer the lac repressor is removed from the operator. This leads to the binding of CAMP to DNA as the CAMP levels are high. It helps in high transcription levels b binding RNA polymerase to promotor.

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How is sea otters interacting with the biotic and abiotic factors in the kelp forest?​
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Brown eyes in humans is a dominant trait. We inherit dominant traits from our parents, some from our mother and some from our
Vsevolod [243]

Answer:e first variant is termed dominant and the second recessive. This state of having two different variants of the same gene on each chromosome is originally caused by a mutation in one of the genes, either new (de novo) or inherited. The terms autosomal dominant or autosomal recessive are used to describe gene variants on non-sex chromosomes (autosomes) and their associated traits, while those on sex chromosomes (allosomes) are termed X-linked dominant, X-linked recessive or Y-linked; these have an inheritance and presentation pattern that depends on the sex of both the parent and the child (see Sex linkage). Since there is only one copy of the Y chromosome, Y-linked traits cannot be dominant nor recessive. Additionally, there are other forms of dominance such as incomplete dominance, in which a gene variant has a partial effect compared to when it is present on both chromosomes, and co-dominance, in which different variants on each chromosome both show their associated traits.

Dominance is not inherent to an allele or its traits (phenotype). It is a strictly relative effect between two alleles of a given gene of any function; one allele can be dominant over a second allele of the same gene, recessive to a third and co-dominant with a fourth. Additionally, one allele may be dominant for one trait but not others.

The blood type of a human is determined by a gene that creates an A, B, AB or O blood type and is located in the long arm of chromosome nine. There are three different alleles that could be present at this locus, but only two can be present in any individual, one inherited from their mother and one from their father.[7]

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Dominance differs from epistasis, the phenomenon of an allele of one gene masking the effect of alleles of a different gene

Explanation:

7 0
3 years ago
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