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Novay_Z [31]
3 years ago
11

Galactosemia is an inherited genetic condition.Children with this condition cannot break down the sugar galactose, which is part

of lactose. Based on the pedigree chart, is this condition a dominant or a recessive disorder
Biology
2 answers:
natulia [17]3 years ago
4 0

Plato answer:

It is recessive. Both parents are heterozygous for the trait, but they do not exhibit the disease themselves. If it were a dominant gene, both parents would have the disease if they carried the gene for it.

Rasek [7]3 years ago
3 0
Human genetics is the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.

Genes can be the common factor of the qualities of most human-inherited traits. Study of human genetics can be useful as it can answer questions about human nature, understand the diseases and development of effective disease treatment, and understand genetics of human life. This article describes only basic features of human genetics; for the genetics of disorders please see: medical genetics.

Galactosemia is an autosomal recessive hereditary disorder caused by a deficiency of the enzyme galactose-1- phosphate uridyl transferase (GALT) that is needed for the breakdown of the milk sugar, galactose.







Representation of the double helix structure of human DNA

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When you talk together in a group during a laboratory exercise, you are engaging in public scientific communication. classroom s
egoroff_w [7]

Answer:

Option number 2 is correct. When you talk together in a group during a laboratory exercise, you are engaging in classroom scientific communication.

Explanation:

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If a scientist talks about any science topic to the public, then it would be a public scientific communication. A scientific communication made among scientists would be termed as professional scientific communication. Any science based communication that is made and kept private would be termed as private scientific communication.

Hence, option 2 is correct. A science based communication between students in a lab would be classroom scientific communication.

6 0
3 years ago
Read 2 more answers
Make a list of 3 advantages of plotting data in graphic form?
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4 0
3 years ago
1) Why is the epicenter of the earthquake limited to two locations after you have data for him to seismograph stations?
frez [133]

Answer:

Answer for question 2:

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Explanation:

7 0
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Only the constituents of amino acids and proteins​
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4 0
3 years ago
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Can anyone tell me the ratio of the genotype and phenotype ???
iogann1982 [59]
<h2>Hey There!</h2><h2>_____________________________________</h2><h2>Answer:</h2><h2>_____________________________________</h2><h2>Phenotype:</h2>

It is the physical appearance of the trait, whether the person has smooth chin or cleft chin.

<h2>Genotype:</h2>

A genotype refers to the genetic characteristics of an organism's trait, if it is heterozygous or hom.ozygous, recessive or dominant.

<h2>_____________________________________</h2><h2>Alleles:</h2>

Cleft chin C is dominant over smooth chin c

<h2>Genotypes of Parents:</h2><h3>FATHER:</h3>

Father has smooth chin thus, it is hom.ozygous recessive i.e. cc

<h3>MOTHER:</h3>

Mother has cleft chin, since cleft chin is dominant there are two possibilities of her genotype,

                           Heterozygous Dominant : Cc

                           Hom.zygous Dominant : CC

but if we cross the hom.zygous fominant mother to hom.ozygous recessive father we will get all the offsprings with the same genotype phenotype so it is not possibile, So the mother is HETEROZYGOUS DOMINANT Cc

<h2>_____________________________________</h2><h2><u>Question</u>:</h2><h2>_____________________________________</h2><h2>Genotypes of Parents:</h2>

FATHER: cc (Hom.ozygous Recessive)

MOTHER: Cc (Heterozygous Dominant)

<h2>_____________________________________</h2><h2>Punnet Square:</h2>

Picture attached!

Picture no 1: it is the cross between hom.ozygous recessive father and hom.ozygous dominant mother and all the offsprings are same both phenotypic and genotypic way so IT IS NOT POSSIBILE

Picture no 2: Its cross between hom.ozygous recessive father and heterozygous dominant mother and there are hybrid and pure recessive both type of offsprings present thus IT IS POSSIBLE!

<h2>_____________________________________</h2><h2>Genotype Ratio of the Offspring:</h2>

Hybrid : Pure Recessive

2 : 2 or 1 : 1

<h2>_____________________________________</h2><h2>Phenotype Ratio of the Offspring:</h2>

Cleft Chin : Smooth Chin

2 : 2 or 1 : 1

<h2>_____________________________________</h2><h2>Best Regards,</h2><h2>'Borz'</h2><h2 />

5 0
3 years ago
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