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Rare Diseases Volume 1, 2013 - Issue 1

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Addendum

Common skeletal features in rare diseases

New links between ciliopathies and FGF-related syndromes

Basil Z Yannakoudakis Department of Craniofacial Development and Stem Cell Biology; King’s College London; London, UK

Karen J Liu Department of Craniofacial Development and Stem Cell Biology; King’s College London; London, UKCorrespondence[email protected]

Article: e27109 | Received 19 Aug 2013, Accepted 06 Nov 2013, Published online: 11 Nov 2013

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https://doi.org/10.4161/rdis.27109

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Articles from other publishers (4)

Eva Hruba, Michaela Kavkova, Linda Dalecka, Miloš Macholan, Tomas Zikmund, Miroslav Varecha, Michaela Bosakova, Jozef Kaiser, Pavel Krejci, Maria Hovorakova & Marcela Buchtova. (2021) Loss of Sprouty Produces a Ciliopathic Skeletal Phenotype in Mice Through Upregulation of Hedgehog Signaling. Journal of Bone and Mineral Research 36:11, pages 2258-2274.
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Paul N. Adler & John B. Wallingford. (2017) From Planar Cell Polarity to Ciliogenesis and Back: The Curious Tale of the PPE and CPLANE proteins. Trends in Cell Biology 27:5, pages 379-390.
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Jing Ma, Fei Liu, Xin Du, Duan Ma & Likuan Xiong. (2017) Changes in lncRNAs and related genes in β-thalassemia minor and β-thalassemia major. Frontiers of Medicine 11:1, pages 74-86.
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Jacqueline M. Tabler, Christopher P. Rice, Karen J. Liu & John B. Wallingford. (2016) A novel ciliopathic skull defect arising from excess neural crest. Developmental Biology 417:1, pages 4-10.
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