Answered: Identify one human trait, other than…

Science

Biology

Identify one human trait, other than skin tone, eye color and stature, that you think has a clinal distribution.

Nutrition Through The Life Cycle

7th Edition

ISBN:9781337919333

Author:Brown, Judith E.

Publisher:Brown, Judith E.

Chapter2: Preconception Nutrition

Section: Chapter Questions

Problem 11RQ: Match the term listed in Column A with its definition from Column B

See similar textbooks

Related questions

Q: Children with this condition has the following features: wide or web-like neck; low-set ears; broad…

A: There are various different kinds of genetic abnormalities that are found in Humans. Some defects…

Q: s alternative form of a single gene is known as parental, dihybrid, reciprocal, allele, or…

A: Alleles are variant forms of a gene. Individuals receive one allele from the father and one from the…

Q: Monozygotic twins: Question 2 options: a) Share 50% of their genetic material and if one twin…

A: Genes are the basic structural and functional units of heredity. They are composed of DNA and they…

Q: The frequency of spina bifida (SB) in the US is 0.002. John has married Mary. There is no family…

A: International occurrence. The average worldwide incidence of spina bifida is 1 case per 1000 births,…

Q: Describe two ways to prevent getting an STI.

A: There are various routes by which a disease is transmitted from an infected individual to a healthy…

Q: If there is no treatment for albinism, what is the status of research on this genetic disorder?…

A: Introduction :- Albinism is an uncommon set of hereditary illnesses characterised by a lack of…

Q: The fraternal birth order effect, in which the number of brothers a boy's mother carried before him…

A: Introduction Birth order refers to the position of a child in a family relative to their siblings.…

Q: In a particular family, children of a diseased mother are all affected, and their maternal…

A: Defective genes cause such mutations or disorders that run down the family and members. Such…

Q: What is the term that describes an individual who expresses a specific phenotype or disease?

A: The term that describes an individual who expresses a specific phenotype or disease is Expressivity.…

Q: ISB 603 Karyotype #5 designation: (hint: this is not a deletion) Genetic condition:

A: Step 1: Step 2: Step 3: Step 4:

Q: Sickle cell disease (SCD) affects millions of people throughout the world; the CDC "Centers for…

A: Detailed explanation:Sickle cell disease (SCD) is a genetic disorder characterized by abnormal…

Q: Hereditary hemochromatosis is an autosomal recessive genetic disorder that causes the body to absorb…

A: Mutations are alterations in the DNA sequence of an organism. Small changes, such as adding or…

Q: Explain what the inheritance of acquired characteristics is.

A: Genetic information is passed from one generation to subsequent generations through inheritance. The…

Q: Explain the following term: Homozygous:

A: Chromosomes are filamentous bodies found in the nucleus. They are composed of DNA (deoxyribonucleic…

Q: The presence of certain factors in a person’s genetic makeup that increase the likelihood of…

A: The genetic arrangement is something that matters greatly to a person’s characteristic makeup. It is…

Q: Cystic fibrosis is chracterized by: 1) Heterozygous expression of an autosomal recessive trait 2)…

A: Cystic fibrosis is a condition which damages the lungs as well as the pancreas in the GI system of a…

Q: Having dimples (D) is dominant over not having dimples (d). A dimpled woman (whose father had no…

A: According to guidelines we have to answer the first 3 sub-parts only. so please kingly post the…

Q: Explain the nondisjunction event that would cause a Turneror Klinefelter syndrome individual.

A: Nondisjunction refers to the failure of homologus chromosomes or sister chromatid to separate during…

Q: Maria (AA-) and Jason (AB+) Phillips had twins, a boy and a girl. Lily (AO-) and Charles (AO-) Smith…

A: The ABO blood group system is present in the human. There are four blood groups in the ABO blood…

Q: Recessive genetic disorders are more frequent than disorders inherited as dominant because : a)…

A: Recessive genetic disorders are genetic conditions which can cause disease in an individual only…

Q: What is syndrome ? Name three syndromes

A: Disease is defined as any deviation from the normal physiologic function or structure of organism.…

Q: a) explain why a diagnosis of ASD is not possible in young babies. b) Given the current…

A: Diagnosis of ASD is not possible in young babies.The reasons are shown below.Behavioral indicators…

Q: Please help True or false, if false rewrite the statement in a way that makes it true. a) A cell…

A: A cell can be defined as the basic structural, functional, and biological unit of all known living…

Q: Define and illustrate the concept of homology using an example.

A: Evolution: Evolution is a systemic process which is happening step by step manner to select an…

Q: Two groups of participants read a description of a person called Mark, who was described as shy,…

A: Human Judgment refers to an attempt to create a hierarchy of better than and less than, superior to…

Q: What category of genetic disorders does albinism disord

A: Answer Albinism is a single gene defect and it is a type genetical disorder.

Q: Based on the testing outcome, give your opinion on whether you think Cystic Fibrosis is a dominant…

A: Cystic fibrosis is a genetic disease in which CFTR gene is mutated. This gene codes a protein…

Q: Write brief summaries (no longer than three lines) on each of the following topics:…

A: What:- Manchester specific markers are digital frequency modulation in which data and clock signals…

Q: mia is caused by gene mutation and transmitted by a recessive allele. Which genotype allows an…

A: Mutation are also known as the sudden changes that causes defects in the genes. A change in one or…

Q: Marfan syndrome is transmitted by a dominant gene.State the probability that a child with an…

A: Marfan syndrome affects the essential parts of the human body, including the bone, eyes, nervous…

Q: What is genetic disorders? Explain by giving an example.

A: Genetics is described as the branch of biology that focuses on the study of genes, their…

Q: Can Turner syndrome be cured?

A: The genetic condition characterized by the absence of an X chromosome in the females. The ploidy of…

Q: a) A man with red-green colour blindness is married to a girl with normal colour vision. What is the…

A: Genetics is the study of the functioning and main codes of variation and heredity. Inheritance is…

Q: Plssssssss helppppp, What are the symptoms of Down syndrome and what is the long term prognosis is…

A: Down's syndrome is a genetic disorder which is caused when abnormal cell division results in extra…

Q: CYSTIC FIBROSIS is an autosomal dominant. It affects both sexes and can skip generations through…

A: A genetic condition is a health issue caused by one or more genetic defects. A single or multiple…

Q: Neurofibromatosis type 1 (NF1) is an inherited is an inheritent dominant disorder. The phenotype…

A: Neurofibromatosis (NF) is a genetic neurological disorder that can affect the brain, spinal cord,…

Q: Recessive genetic disorders are more frequent than disorders inherited as dominant because : a)…

A: Genetics is a branch of biology, which focuses on the study of genes, genetic variations, and…

Q: Huntington disease (HD) is a genetic disorder that usually first appears in middle age and, over…

A: Huntington disease (HD) is a progressive brain disorder that causes uncontrolled movements,…

Q: If a person has albinism and dark skinned parents what is their genotype

A: Albinism results from the mutation in several genes. It follows the autosomal recessive inheritance…

Question

Identify one human trait, other than skin tone, eye color and stature, that you think has a clinal distribution.

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 steps

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.

Similar questions

In a particular family, children of a diseased mother are all affected, and their maternal grandmother was also affected. But the cousins (children of maternal uncle) are not affected. No disorders were recorded in the paternal side. Can you identify the type of this disorder and provide justifications in support of your identification?
In medical terms, what is an eponym and do you know some examples?
1 6 13 19 | }H_IC K 2 7 14 20 8 15 3 21 22 10 16 H 11 17 X What is this type of image called? How are they useful? What disorder does this person have? How can you tell? What is the birth gender of this individual? 5 12 18 Y
Jonah and Jana are siblings. Jonah has the genetic disorder cystic fibrosis, caused by inheriting one copy from each parent of a mutation in the CF gene. Jana does not have cystic fibrosis. Which of the following statements is/are true? (Select all that are true) a)Jana does not have the gene that when mutant causes cystic fibrosis. b)Jana has the gene that when mutant causes cystic fibrosis. c)Jana has two copies of the allele that causes cystic fibrosis. d)Jana does not have two copies of the allele that causes cystic fibrosis.
What does the acronym TPA stand for and how is TPA used in diagnostic medicine? Explain 2-3 sentences
Draw a Punnett square for a mother that is a carrier of hemophilia and a father that is not affected. Use the paperclip icon to attach your image.
If a condition is a “genetic” disorder, what does that mean and how would it be different from a non genetic disorder?
Jane (mother): Tt XcXc IBi -Taster, Color-blind female, Blood type B John (father): tt XcY IAIB- Non-taster, Color-blind male, Blood type AB Explain whether or not these two parents could possibly produce a normal visioned child who has blood type O? Explain whether or not these two parents could possibly produce a color blind child, who could not taste PTC paper, and has blood type A? What blood types could the children of this couple possibly have? How many phenotypically different "kinds" of children could this couple produce? List a maximum of eight phenotypes. Sorry for asking so many questions but they are related. Please I need your help in a few minutes.
Huntington chorea is an inherited disorder, with children of a parent with the disorder having a 50% chance of developing the disease. An individual with the disease usually does not manifest symptoms until he or she is between 30 and 45 years of age. The disease then progresses to death over the next 10 to 15 years. If a child of an affected parent has not developed symptoms by the age of 45, it is not likely that the symptoms will ever develop. Discuss your thinking process when deciding whether you would or would not choose to have the testing to know if you will develop Huntington chorea.
Draw a line to label the major parts of the following.
Answer the question(s) in reference to the five disorders listed below: Hutchtinson-Gilford progeria hemophilia turner syndrome down syndrome klinefelter syndrome
a) What does SVT stand for? b) When should the term SVT be used? 14.