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(Continued from page 10)
Let's go back to the scientists and the DNA for a moment before we go any further. While they did not use chromosomal DNA to identify the remains unearthed in Koptyaki they did use it to determine the gender of the bones. To do this the scientists must see if the DNA contains two X-chromosomes indicating a female or one X and one Y-chromosome indicating a male. One can assume that since the gene that causes haemophilia is part of the X-chromosome that was used to identify the gender of the remains the scientists would be able to recognize it. If that is the case, one can also assume that they already know for certain if the Empress and her daughters really were carriers of the disease.
No evidence of such a type, which could prove the existence of haemophilia in the Royal line, has ever been published. If the chromosomal DNA examination did reveal such evidence then the scientists are keeping it to themselves. Logic dictates that the only reason for withholding such evidence is if it showed that the haemophilia gene is not present in the remains of the Romanov women. That, in turn, would mean that the blood disease suffered by the Tsarevich was something else. The only reason to withhold such information would be if there is concern about an Alexei claimant who fits that description.
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