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<xml>
<records>
<record>
  <contributors>
    <authors>
      <author>Cucco, F.</author>
      <author>Sarogni, P.</author>
      <author>Rossato, S.</author>
      <author>Alpa, M.</author>
      <author>Patimo, A.</author>
      <author>Latorre, A.</author>
      <author>Magnani, C.</author>
      <author>Puisac, B.</author>
      <author>Ramos, F.J.</author>
      <author>Pié, J.</author>
      <author>Musio, A.</author>
    </authors>
  </contributors>
  <titles>
    <title>Pathogenic variants in EP300 and ANKRD11 in patients with phenotypes overlapping Cornelia de Lange syndrome</title>
    <secondary-title>Am. J. Med. Genet. A</secondary-title>
  </titles>
  <doi>10.1002/ajmg.a.61611</doi>
  <pages/>
  <volume/>
  <number/>
  <dates>
    <year>2020</year>
    <pub-dates>
      <date>2020</date>
    </pub-dates>
  </dates>
  <abstract/>
</record>

</records>
</xml>