Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome)
- 1 January 2013
- journal article
- letter
- Published by Wiley in Clinical Genetics
- Vol. 83 (1), 92-95
- https://doi.org/10.1111/j.1399-0004.2012.01880.x
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
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- Ciliogenesis: building the cell's antennaNature Reviews Molecular Cell Biology, 2011
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- Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner SyndromeAmerican Journal of Human Genetics, 2010
- Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 GeneAmerican Journal of Human Genetics, 2010
- An unclassifiable short rib‐polydactyly syndrome with acromesomelic hypomineralization and campomelia in siblingsAmerican Journal of Medical Genetics Part A, 2007