FIGURE 1
FROM:
Skewed X chromosome inactivation in carriers is not a constant finding in FG syndrome
Martine Raynaud, Sabine Dessay, Nathalie Ronce, John Opitz, Marcus Pembrey, Corrado Romano, Claude Moraine and Sylvain Briault
BACK TO ARTICLEFigure 1.
There are at least three gene localizations for FG syndrome: FGS1 (Xq12-Xq21.31), FGS2 (Xq11 or Xq28) and FGS3 (Xpter-Xp22.3).
