Hello, please please help me with this, I would greatly appreciate it!!!!
THANK YOU SO MUCH!!!
Homework Answers
Question 3
A.X-linked dominant.because from the affected father in 2nd generation the defective x chromosome pass to every female child and they are expressing the disease.And male child are not affected as they have normal x choromosome from mother.
B.autosomal recessive.both parents are Carrier of the disease.and there defective allele accumulated in one child of next generation.
c.autosomal dominant.the normal child due to accumulation of normal alleles from both parents.
D.x linked recessive disease. That's why all the male child in the 3rd generation showing the disease.And the mother of 1st generation may be carrier ca the disease so that affected x chromosome get accumulated with affected father x chromosome and create affected female child in 2nd generation.
Question 4
Autosomal recessive inheritance-c
Autosomal dominant inheritance-a
X linked recessive inheritance-b
X linked dominant inheritance-d
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Hello, please please help me with this, I would greatly
appreciate it!!!!
THANK YOU SO MUCH!!!...
Look carefully at the pedigrees below and: 1) indicate whether the transmission appears autosomal or sex-linked...
Look carefully at the pedigrees below and:
1) indicate whether the transmission appears autosomal or
sex-linked
2) indicate whether the transmission appears dominant or
recessive
3) provide at least two characteristics for each that support
your conclusion.
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at...
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance:...
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at once among several members of one generation (siblings) *** Autosomal dominant inheritance each affected individual has an affected parent -when one parent is affected, transmission to the offspring (on average) *** -two unaffected parents do not transmit...
The conclusions about inheritance (above) can be used to help analyze pedigrees. For each pedigree below,...
The conclusions about inheritance (above) can be used to help analyze pedigrees. For each pedigree below, tell if the trait can be autosomal dominant, autosomal recessive, and X-linked recessive. If the pedigree cannot fit a mode of inheritance, tell why. Record your answers in the table on the next page. Pedigree A 2 3 o.a. 9 10 12 (13 14 ad ada 15 16 Xx 20 aa ia ha Pedigree B 910 11 12 14 a ta da Enter either...
Part B Determining genotypes in pedigrees of X-linked conditions The pedigree from Part A is shown...
Part B Determining genotypes in pedigrees of X-linked
conditions
The pedigree from Part A is shown below. Fill in the most likely
genotypes of the indicated individuals in the pedigree. Note that a
dominant allele followed by an underscore (_) indicates that either
the dominant or the recessive allele may be present at the second
position. Drag one pink label (for condition A, autosomal
recessive) to each pink target. Drag one blue label (for condition
B, X-linked recessive) to each...
A man with a specific unusual genetic trait (leading to heterozygosity) is house with an unaffected...
A man with a specific unusual genetic trait (leading to
heterozygosity) is
house with an unaffected and non-carrying woman, and they have four
children. The pedigrees of
this family is shown in graphs a-e. For each inheritance mode
indicate
how many children of each sex will express the trait (color those
affected in each tree
genealogical according to the type of inheritance).
a) Autosomal recessive trait:
b) Autosomal dominant trait:
c) X-linked recessive trait:
d) X-linked dominant trait:
e) Trait...
For each pedigree below determine the most likely mode of inheritance and label each individual with...
For each pedigree below determine the most likely mode of
inheritance and label each individual with a genotype. If you know
they have a dominant phenotype, but don’t know the genotype, then
label them with both possibilities. Please use the alleles A and a
for autosomal modes of inheritance and XA, Xa and Ya for any types
of sex-linkage (note: an “a” is only on the Y if the trait is
Y-linked). Modes of inheritance are autosomal dominant, autosomal
recessive,...
please help me!!! best will be rated 1. (20 points) a. The short pedigree below shows...
please help me!!! best will be rated
1. (20 points) a. The short pedigree below shows affected individuals in this family in red. Which modes of inheritance (X-linked recessive, X-linked dominant, Y-linked, autosomal recessive, autosomal dominant) can be ruled out, and which mode is most likely? b. (10 points) What is the likelihood that child A will be affected? Child B? O ■ ● Co
Please help me understand this. with best desenbes the mode of inheritance in the pedigree shown...
Please help me understand this.
with best desenbes the mode of inheritance in the pedigree shown below? wint in problems like these, solve the pedigree by identifying genotypes of all individuals shown for EACH of the inheritance catterns separately. You will find contradictions (individuals that cannot have the genotype you identified for all except one type of inheritance pattern. The inheritance pattern that produces no contradictions must be the correct answer 0 .0 d . 00 bodo Select one: a....
2. Analysis of a breeding history in pureb eding history in purebred dogs revealed a familial...
2. Analysis of a breeding history in pureb eding history in purebred dogs revealed a familial disease impacting some animals. Pedigree below shows the inheritance pattern in the breeding population. a) For each mode of inheritance listed below, indicate whether it is: 1: likely, 2: possible, or 3: impossible. You may make the following simplifying assumptions: 1) disease alleles are rare among animals in the general population; 2) only mothers contribute mitochondria; 1) Autosomal, sex influenced, dominant in males/recessive in...
What is the mode of inheritance for hypercholesterolemia? a. Autosomal dominant b. Autosomal recessive c. X-linked...
What is the mode of inheritance for hypercholesterolemia?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible
----------------------------------------------------------------
What is the mode of inheritance for Hunter's syndrome?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible.
------------------------------------------------------------
What is the genotype for individual II-3 at the
hypercholesterolemia locus (dominant allele is denoted by H,
recessive allele...
Look carefully at the pedigrees below and:
1) indicate whether the transmission appears autosomal or
sex-linked
2) indicate whether the transmission appears dominant or
recessive
3) provide at least two characteristics for each that support
your conclusion.
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at...
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at once among several members of one generation (siblings) *** Autosomal dominant inheritance each affected individual has an affected parent -when one parent is affected, transmission to the offspring (on average) *** -two unaffected parents do not transmit...
The conclusions about inheritance (above) can be used to help analyze pedigrees. For each pedigree below, tell if the trait can be autosomal dominant, autosomal recessive, and X-linked recessive. If the pedigree cannot fit a mode of inheritance, tell why. Record your answers in the table on the next page. Pedigree A 2 3 o.a. 9 10 12 (13 14 ad ada 15 16 Xx 20 aa ia ha Pedigree B 910 11 12 14 a ta da Enter either...
Part B Determining genotypes in pedigrees of X-linked
conditions
The pedigree from Part A is shown below. Fill in the most likely
genotypes of the indicated individuals in the pedigree. Note that a
dominant allele followed by an underscore (_) indicates that either
the dominant or the recessive allele may be present at the second
position. Drag one pink label (for condition A, autosomal
recessive) to each pink target. Drag one blue label (for condition
B, X-linked recessive) to each...
A man with a specific unusual genetic trait (leading to
heterozygosity) is
house with an unaffected and non-carrying woman, and they have four
children. The pedigrees of
this family is shown in graphs a-e. For each inheritance mode
indicate
how many children of each sex will express the trait (color those
affected in each tree
genealogical according to the type of inheritance).
a) Autosomal recessive trait:
b) Autosomal dominant trait:
c) X-linked recessive trait:
d) X-linked dominant trait:
e) Trait...
For each pedigree below determine the most likely mode of
inheritance and label each individual with a genotype. If you know
they have a dominant phenotype, but don’t know the genotype, then
label them with both possibilities. Please use the alleles A and a
for autosomal modes of inheritance and XA, Xa and Ya for any types
of sex-linkage (note: an “a” is only on the Y if the trait is
Y-linked). Modes of inheritance are autosomal dominant, autosomal
recessive,...
please help me!!! best will be rated
1. (20 points) a. The short pedigree below shows affected individuals in this family in red. Which modes of inheritance (X-linked recessive, X-linked dominant, Y-linked, autosomal recessive, autosomal dominant) can be ruled out, and which mode is most likely? b. (10 points) What is the likelihood that child A will be affected? Child B? O ■ ● Co
Please help me understand this.
with best desenbes the mode of inheritance in the pedigree shown below? wint in problems like these, solve the pedigree by identifying genotypes of all individuals shown for EACH of the inheritance catterns separately. You will find contradictions (individuals that cannot have the genotype you identified for all except one type of inheritance pattern. The inheritance pattern that produces no contradictions must be the correct answer 0 .0 d . 00 bodo Select one: a....
2. Analysis of a breeding history in pureb eding history in purebred dogs revealed a familial disease impacting some animals. Pedigree below shows the inheritance pattern in the breeding population. a) For each mode of inheritance listed below, indicate whether it is: 1: likely, 2: possible, or 3: impossible. You may make the following simplifying assumptions: 1) disease alleles are rare among animals in the general population; 2) only mothers contribute mitochondria; 1) Autosomal, sex influenced, dominant in males/recessive in...
What is the mode of inheritance for hypercholesterolemia?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible
----------------------------------------------------------------
What is the mode of inheritance for Hunter's syndrome?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible.
------------------------------------------------------------
What is the genotype for individual II-3 at the
hypercholesterolemia locus (dominant allele is denoted by H,
recessive allele...
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