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

Author:

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

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference44 articles.

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4. New syndrome of skeletal, dental and hair anomalies;Sensenbrenner;Birth Defects Orig. Artic. Ser.,1975

5. Asphyxiating thoracic dystrophy with familial characteristics;Jeune;Arch. Fr. Pediatr.,1955

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