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Advances in technology such as personal computers and cellul…

Advances in technology such as personal computers and cellular telecommunications are indicated in the supply graph by a movement along the supply curve

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In the image below, which letters represent the 5’ ends of t…

In the image below, which letters represent the 5’ ends of the DNA (i.e., A, B, C or D).   

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Which of the following organelles contains extranuclear DNA?

Which of the following organelles contains extranuclear DNA?

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An individual has a reciprocal translocation involving chrom…

An individual has a reciprocal translocation involving chromosomes 1 and 2. The chromosomes involved in the translocation, and their normal homologs, form a translocation cross during meiosis as shown below. Regarding gamete production, which outcome can give rise to viable gametes (i.e., gametes that give rise to live offspring)? (Think about which outcome produces gametes with a balanced amount of genetic material).    

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When packaging DNA into chromosomes, place the following lev…

When packaging DNA into chromosomes, place the following levels of chromosome organization in the correct order from the least compacted structure to the most compacted structure. I. Heterochromatin II. Radial loop domain III. DNA double helix IV. 30 nm fiber V. Nucleosome

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Please show both sides of your scratch paper to the camera b…

Please show both sides of your scratch paper to the camera before submitting. Approximately 75% of cases of Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are caused by a deletion of a small region on chromosome 15 that contains a cluster of imprinted genes. The gene that causes PWS when deleted is normally maternally imprinted (paternally expressed) and the gene that causes AS when deleted is usually paternally imprinted (maternally expressed). If Richard inherits a chromosome 15 with the deletion from his father, what will be Richard’s phenotype?

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The pedigree below shows the inheritance of a mitochondrial…

The pedigree below shows the inheritance of a mitochondrial disorder. What is the most likely mode of inheritance for this mitochondrial disorder? Assume complete penetrance.  

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The gene for nail patellar syndrome (n = normal allele; N  =…

The gene for nail patellar syndrome (n = normal allele; N  = mutant allele) shows linkage to the blood group A, B and O alleles (IA = blood type A; IB = blood type B; i = blood type O). The IA and IB alleles both show complete dominance over the i allele. The IA and IB alleles are co-dominant to each other. The two genes are located 20 m.u. apart. Beth has the genotype n____i   N____IA Simon has the genotype    N____i  n____IB What is the probability that they will have a normal child who is blood type B? 

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Which of the following base pairings is normally found in DN…

Which of the following base pairings is normally found in DNA?  

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Given the following sequence of genes on a chromosome, what…

Given the following sequence of genes on a chromosome, what change in chromosome structure occurred (the * indicates the centromere)? before A B C D * E F G H    after    A B C D * E F E F G H   

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