Sickle-cell disease is a chronic, inherited anemia and it is caused by a mutation in the hemoglobin protein coding gene. Hemoglobin carries oxygen and the gene coding for hemoglobin protein is located on the chromosome 11. The sickle-cell disease is an autosomal recessive genetic disorder, in which red blood cells (RBC) sickle, plugging small blood vessels. The normal hemoglobin allele ( H ) dominates the sickle cell allele ( h ). The recessive allele is responsible for the sickle-cell disease. An individual carrying two recessive alleles ( hh ) can result in sickle-cell disease. The carrier contains one dominant ( H ) allele and one recessive allele ( h ).

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Chapter 8, Problem 8TQ

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Sickle-cell disease is a chronic, inherited anemia and it is caused by a mutation in the hemoglobin protein coding gene. Hemoglobin carries oxygen and the gene coding for hemoglobin protein is located on the chromosome 11. The sickle-cell disease is an autosomal recessive genetic disorder, in which red blood cells (RBC) sickle, plugging small blood vessels. The normal hemoglobin allele (H) dominates the sickle cell allele (h). The recessive allele is responsible for the sickle-cell disease. An individual carrying two recessive alleles (hh) can result in sickle-cell disease. The carrier contains one dominant (H) allele and one recessive allele (h).

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Answer 2

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Chapter 8, Problem 8TQ

Summary Introduction

Sickle-cell disease is a chronic, inherited anemia and it is caused by a mutation in the hemoglobin protein coding gene. Hemoglobin carries oxygen and the gene coding for hemoglobin protein is located on the chromosome 11. The sickle-cell disease is an autosomal recessive genetic disorder, in which red blood cells (RBC) sickle, plugging small blood vessels. The normal hemoglobin allele (H) dominates the sickle cell allele (h). The recessive allele is responsible for the sickle-cell disease. An individual carrying two recessive alleles (hh) can result in sickle-cell disease. The carrier contains one dominant (H) allele and one recessive allele (h).

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Answer 3

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Chapter 8, Problem 8TQ

Summary Introduction

Sickle-cell disease is a chronic, inherited anemia and it is caused by a mutation in the hemoglobin protein coding gene. Hemoglobin carries oxygen and the gene coding for hemoglobin protein is located on the chromosome 11. The sickle-cell disease is an autosomal recessive genetic disorder, in which red blood cells (RBC) sickle, plugging small blood vessels. The normal hemoglobin allele (H) dominates the sickle cell allele (h). The recessive allele is responsible for the sickle-cell disease. An individual carrying two recessive alleles (hh) can result in sickle-cell disease. The carrier contains one dominant (H) allele and one recessive allele (h).

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Answer 4

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Chapter 8, Problem 8TQ

Summary Introduction

Sickle-cell disease is a chronic, inherited anemia and it is caused by a mutation in the hemoglobin protein coding gene. Hemoglobin carries oxygen and the gene coding for hemoglobin protein is located on the chromosome 11. The sickle-cell disease is an autosomal recessive genetic disorder, in which red blood cells (RBC) sickle, plugging small blood vessels. The normal hemoglobin allele (H) dominates the sickle cell allele (h). The recessive allele is responsible for the sickle-cell disease. An individual carrying two recessive alleles (hh) can result in sickle-cell disease. The carrier contains one dominant (H) allele and one recessive allele (h).

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Answer 5

Chapter 8, Problem 8TQ

Summary Introduction

Sickle-cell disease is a chronic, inherited anemia and it is caused by a mutation in the hemoglobin protein coding gene. Hemoglobin carries oxygen and the gene coding for hemoglobin protein is located on the chromosome 11. The sickle-cell disease is an autosomal recessive genetic disorder, in which red blood cells (RBC) sickle, plugging small blood vessels. The normal hemoglobin allele (H) dominates the sickle cell allele (h). The recessive allele is responsible for the sickle-cell disease. An individual carrying two recessive alleles (hh) can result in sickle-cell disease. The carrier contains one dominant (H) allele and one recessive allele (h).

Answer 6

Chapter 8, Problem 8TQ

Summary Introduction

Sickle-cell disease is a chronic, inherited anemia and it is caused by a mutation in the hemoglobin protein coding gene. Hemoglobin carries oxygen and the gene coding for hemoglobin protein is located on the chromosome 11. The sickle-cell disease is an autosomal recessive genetic disorder, in which red blood cells (RBC) sickle, plugging small blood vessels. The normal hemoglobin allele (H) dominates the sickle cell allele (h). The recessive allele is responsible for the sickle-cell disease. An individual carrying two recessive alleles (hh) can result in sickle-cell disease. The carrier contains one dominant (H) allele and one recessive allele (h).

Answer 7

Chapter 8, Problem 8TQ

Summary Introduction

Sickle-cell disease is a chronic, inherited anemia and it is caused by a mutation in the hemoglobin protein coding gene. Hemoglobin carries oxygen and the gene coding for hemoglobin protein is located on the chromosome 11. The sickle-cell disease is an autosomal recessive genetic disorder, in which red blood cells (RBC) sickle, plugging small blood vessels. The normal hemoglobin allele (H) dominates the sickle cell allele (h). The recessive allele is responsible for the sickle-cell disease. An individual carrying two recessive alleles (hh) can result in sickle-cell disease. The carrier contains one dominant (H) allele and one recessive allele (h).

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Ch. 8 - Prob. 1TQ Ch. 8 - Prob. 2TQ Ch. 8 - Prob. 3TQ Ch. 8 - Prob. 4TQ Ch. 8 - Prob. 5TQ Ch. 8 - Prob. 6TQ Ch. 8 - Prob. 7TQ Ch. 8 - Prob. 8TQ Ch. 8 - Prob. 9TQ Ch. 8 - Prob. 10TQ

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