Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations

Sheila Unger, Detlef Böhm, Frank J. Kaiser, Silke Kaulfuß, Wiktor Borozdin, Karin Buiting, Peter Burfeind, Johann Böhm, Francisco Barrionuevo, Alexander Craig, Kristi Borowski, Kim Keppler-Noreuil, Thomas Schmitt-Mechelke, Bernhard Steiner, Deborah Bartholdi, Johannes Lemke, Geert Mortier, Richard Sandford, Bernhard Zabel, Andrea Superti-FurgaJürgen Kohlhase*

*Corresponding author for this work
29 Citations (Scopus)

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