If the baby girl has the condition then she got a X chromosome from each parent. And it is known that it is the sex linked form of the disease in this case.Then the mutated X chromosome could have come from either parent. However, we are told that the girl baby has sex linked recessive form which means that the mother has 2 mutated X chromosomes which is extremely unlikely but possible. Here is a quotation about the condition from the National Institutes of Health, " X-linked recessive means that in females, a mutation would have to occur in both copies of a gene to cause the disorder. In males, one altered copy of a gene in each cell is sufficient to cause the condition. Because it is unlikely that females will have two altered copies of a particular gene, males are affected by X-linked recessive disorders much more frequently than females."
So, I would choose answer B, "yes, but the information given is unsure to come to a conclusion"