Deletions in the 3′ Part of the NFIX Gene Including a Recurrent Alu‐Mediated Deletion of Exon 6 and 7 Account for Previously Unexplained Cases of Marshall–Smith Syndrome
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R. Hennekam | A. Shaw | E. Seemanová | M. Zenker | A. Reis | M. Volleth | V. Cormier-Daire | E. Holmberg | J. Vogt | M. Delrue | D. Schanze | P. Meinecke | T. Hasegawa | R. Koenig | A. Dieux-Coeslier | I. Schanze | G. Krüger | Dorothée Neubauer