Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling.
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A. Noegel | S. Lyonnet | C. Becker | F. Escande | P. Wagle | S. White | Susanne Motameny | L. Pais | F. Petit | W. Höhne | G. Baujat | M. Willems | B. Budde | M. S. Hussain | Salem Alawbathani | L. Gallacher | A. Jourdain | S. Manouvrier-Hanu | M. Asif | J. Ghoumid | I. A. Ba-Saddik | C. Vanlerberghe | P. Nürnberg | T. Georgomanolis | William Dufour | S. Alawbathani | M. Hussain