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Tanphaichitr V, Broquist HP
Ayrca rn tercihinde yalnzca kullanc yorumlarna deil, rnn ieriine, formuna ve retici markann gvenilirliine de dikkat edilmesi gerekir
doi: 10.1016/j.cell.2008.02.043 66 IrwinM
Therefore, a copy of the NF1 mutant gene (either parent) is required to cause the syndrome, and the chance of having a child with the autosomal dominant syndrome is 50% for each possible pregnancy
