Answer:
See the answer below
Explanation:
For two normal parents to have produced a daughter who suffers from AGG, <u>it means the disorder is an autosomal recessive trait. In order words, it means the parents are both carrying the allele for the disorder in recessive form</u>.
Let us assume that the allele for the disorder is represented by b, meaning that the alternate form would be B. <u>Both parents will have the genotype Bb</u> and will both appear normal.
Bb x Bb
BB Bb Bb bb
The affected child would be the one with bb genotype while the remaining children would appear normal. See the attached image for the Punnet's square analysis of the cross.
The genotypes of the parent would be heterozygous.
Answer:
Gamma rays
Explanation:
Has the highest energy, the shortest wavelength, and the highest frequency
Lakes are large and loudish, whereas ponds are generally a lot more quiet and steady and small.
Explanation:
The small intestine includes the duodenum, jejunum, and ileum.
Answer:
The correct answer is ''All three are caused by disparate genes, but each gene was found to contain repeats of a unique trinucleotide sequence.''
Explanation:
Four groups of trinucleotide repeats related to DNA expansion have been characterized in the human genome. CGGI GCC, CAGIGTC, CTGIGAC and recently GW CTT sequences. The CGGl GCC sequences are usually located in the noncoding regions of different genes and when expanded they associate with fragile sites on the chromosomes. The CAGIGTC repeats are part of the coding region and are related to different neurodegenerative disorders. You can try to make a classification depending on the unit that is repeated, having on one side a group that are caused by repeats of the CAG trinucleotide (cytosine, adenine, guanine). Huntington's disease (HD) is a progressive disorder of motor, cognitive and psychic function. The disease is inherited in an autosomal dominant manner, and is caused by the expansion of CAG trinucleotide repeats in exon 1 of the gene called huntingtin (HTT or IT-15). Unstable mutations have also been found in which the repeat unit does not is composed of three nucleotides, if not four, such as type 2 myotonic dystrophy, where the tetranucleotide CCTG repeats. Fragile X Syndrome consists of an abnormal expansion of the cytosine-guanine-guanine trinucleotide (CGG) in the FMR1 gene, which prevents intellectual disability and also influences the formation of connective tissue