it is a 50/50 because if you cant get more that 50 % its not
By showing the history of genetics in the family
Its a pedigree. A pedigree shows the inheritance of a genetic disorder within a family and can help to determine the inheritance pattern and whether any particular individual has an allele for that disorder.
A pedigree is used to determine whether you are at risk of inheriting a particular genetic disorder.
Common pedigree and probability problems encountered in genetic studies include determining the likelihood of inheriting a specific trait or disease based on family history, calculating the probability of passing on a genetic mutation to offspring, and analyzing the inheritance patterns of complex traits influenced by multiple genes. These problems often involve using Punnett squares, pedigrees, and probability calculations to understand genetic inheritance patterns.
A Pedigree
You could make a pedigree which could identify carriers of a genetic disorder and individuals with the disorder. You could do blood tests to determine whether a person carries a gene for a particular genetic disorder. You could make a karyotype to determine whether there are any chromosomal abnormalities.
The answer depends on the genes of the parents and further ancestors.
Sex-linked.
The probability would be 0.5 or 50%. A heterozygous woman will pass on the X chromosome with the recessive allele to 50% of her sons, and since the disorder is recessive, the son would only have the disorder if the X chromosome with the recessive allele is inherited from the mother.
It cannot (unless the parents were homozygous), but it can help predict the odds of having a child with a genetic disorder.
E. A. Thompson has written: 'Pedigree analysis in human genetics' -- subject(s): Genetic Models, Human genetics, Human population genetics, Medical genetics, Pedigree, Probability, Statistical methods
Some common problems that can arise when practicing with a pedigree in genetic analysis include incomplete or inaccurate family history information, difficulty in determining the mode of inheritance, small sample sizes leading to unreliable conclusions, and the presence of genetic heterogeneity complicating the analysis.