Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome
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B. Ceulemans | E. Sistermans | A. Groffen | H. Yntema | W. Nillesen | G. Beunders | S. D. de Munnik | E. J. Meijers-Heijboer | N. van der Aa | E. Voorhoeve | R. Frank Kooy