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Ciliopathies with Skeletal Anomalies and Renal Insufficiency due to Mutations in the IFT-A Gene WDR19

✍ Scribed by Cecilie Bredrup; Sophie Saunier; Machteld M. Oud; Torunn Fiskerstrand; Alexander Hoischen; Damien Brackman; Sabine M. Leh; Marit Midtbø; Emilie Filhol; Christine Bole-Feysot; Patrick Nitschké; Christian Gilissen; Olav H. Haugen; Jan-Stephan F. Sanders; Irene Stolte-Dijkstra; Dorus A. Mans; Eric J. Steenbergen; Ben C.J. Hamel; Marie Matignon; Rolph Pfundt; Cécile Jeanpierre; Helge Boman; Eyvind Rødahl; Joris A. Veltman; Per M. Knappskog; Nine V.A.M. Knoers; Ronald Roepman; Heleen H. Arts

Book ID: 113423117
Publisher: American Society of Human Genetics
Year: 2011
Tongue: English
Weight: 822 KB
Volume: 89
Category: Article
ISSN: 0002-9297
DOI: 10.1016/j.ajhg.2011.10.001

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