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Meier–Gorlin syndrome: Growth and secondary sexual development of a microcephalic primordial dwarfism disorder von de Munnik, Sonja A., Otten, Barto J., Schoots, Jeroen, Bicknell, Louise S., Aftimos, Salim, Al‐Aama, Jumana Y., van Bever, Yolande, Bober, Michael B., Borm, George F., Clayton‐Smith, Jill, Deal, Cheri L., Edrees, Alaa Y., Feingold, Murray, Fryer, Alan, van Hagen, Johanna M., Hennekam, Raoul C., Jansweijer, Maaike C.E., Johnson, Diana, Kant, Sarina G., Opitz, John M., Ramadevi, A. Radha, Reardon, Willie, Ross, Alison, Sarda, Pierre, Schrander‐Stumpel, Constance T.R.M., Sluiter, A. Erik, Temple, I. Karen, Terhal, Paulien A., Toutain, Annick, Wise, Carol A., Wright, Michael, Skidmore, David L., Samuels, Mark E., Hoefsloot, Lies H., Knoers, Nine V.A.M., Brunner, Han G., Jackson, Andrew P., Bongers, Ernie M.H.F.
Veröffentlicht in American journal of medical genetics. Part A
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