Question

In: Biology

A male with gigantism (due to paternal duplication of the Igf2 locus on the same chromosome)...

A male with gigantism (due to paternal duplication of the Igf2 locus on the same chromosome) married a normal individual. He worries about having children since they may also have gigantism. What would you tell him?

Question 2 options:

They will be all healthy.

Only sons have 50% chance of developing gigantism.

Children have 50% chance of having gigantism.

Only daughters have 50% chance of developing gigantism.

Solutions

Expert Solution


Related Solutions

            Chromosome Chromosome             Locus Number Locus   Number        &nb
            Chromosome Chromosome             Locus Number Locus   Number                      TPOX 2 TH01 11 D3S1358 3 VWA 12 FGA 4 D13S317 13 D5S818 5 D16S539 16 CSF1PO 5 D18S51 18 D7S820 7 D21S11 21 D8S1179 8 Table 1. Locus Alleles Frequency Locus RMP TPOX                    8 12 0.535 0.041 TH01 10 10 0.008 D3S1358 16 17 0.222 0.222 FGA 21 23 0.0185 0.134 CSF1PO 11 13 0.301 0.096 D8S51 14 19 0.137 0.038 D21S11 28 29 0.159 0.195 If you haven’t already done so, calculate...
Is everyone's paternal gene silenced because of imprinting in that section of chromosome 15 that causes...
Is everyone's paternal gene silenced because of imprinting in that section of chromosome 15 that causes angelman syndrome? (when the other parents gene is silenced and now there is no back up because of imprinting caused by methylation) I'm asking if every typical person has this imprinting for angelman syndrome and vice versa maternally for Prader-willie syndrome I'm getting confused while writing a report. (I need help as soon as possible because I'm writing a report for tomorrow). Thank you!...
Some cancers are consistently associated with the duplication of a particular part of a chromosome. What...
Some cancers are consistently associated with the duplication of a particular part of a chromosome. What type of gene is most likely to be found in the duplicated region?
There are three traits in mice that are found on the same chromosome (they are linked)....
There are three traits in mice that are found on the same chromosome (they are linked). Gray fur is dominant to brown fur, long tails are dominant to short tails, and notched ears are dominant to unnotched ears. A female mouse who is heterozygous is crossed with a male who is homozygous recessive. The observed offspring are shown below: # offspring. fur color. tail length ear shape 372 gray long notched 41 gray short notched 2 gray long unnotched 36...
True or False When genes are on the same chromosome, the alleles on one of the...
True or False When genes are on the same chromosome, the alleles on one of the two homologous chromosomes are considered to be in trans. Two genes can be syntenic and unlinked. If recombination rate is high, then a particular combination of alleles is likely to be transferred to the next generation intact.
Bar is a dominant mutation on the Drosophila X-chromosome. A Bar male crossed to a wildtype...
Bar is a dominant mutation on the Drosophila X-chromosome. A Bar male crossed to a wildtype female giving the following results:             Bar females                 998 wild type males           1021 wild type female               1 Remember: in Drosophila two X-chromosomes make a female fly and one X-chromosome makes a male; the Y is irrelevant.   XXX is lethal. Part I: What are the complete and exact genotypes of each parent and each type of offspring?                female parent:             male parent:...
In humans, the RH factor and elliptocytosis genes are located on the same chromosome at 3%...
In humans, the RH factor and elliptocytosis genes are located on the same chromosome at 3% from each other. The color blindness gene and the night blindness gene are located 40% apart on the X chromosome. Rhesus positivity and elliptocytes - dominant alleles, and night and color blindness are recessive. А) A woman who was heterozygous in all her genes and whose ancestors had no crossing over was married to a man who suffered from night blindness and color blindness,...
This would NOT be found in mitosis: Select one: Cells with the same chromosome number and...
This would NOT be found in mitosis: Select one: Cells with the same chromosome number and identical DNA Sister chromatids Centromere Cells with reduced chromosome number with different DNA Diploid cell Clear my choice This best describes a cell with homologous chromosomes: Select one: A condition where chromosomes are found in an abnormal number in a cell A condition where chromosomes are unpaired, results in a haploid cell A condition where one parent provides two chromosomes to an offspring The...
List the normal pair of sex chromosomes, and possible sex chromosome aneuploidy for male and female,...
List the normal pair of sex chromosomes, and possible sex chromosome aneuploidy for male and female, respectively. And then briefly explain the possible mechanism of XY girls and XX boys.
Genes A, B, and C are located on the same chromosome with following order. Linkage map...
Genes A, B, and C are located on the same chromosome with following order. Linkage map distances among them are 11cM between A and B and 34cM between B and C. 1. When two parental genotypes were ABC/abc and abc/abc and there were 500 offspring, what would be the possible/expected genotypes and their numbers among the offspring? Assume there was no interference.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT