Journal Articles
Clinical Genetics
Year : 2017
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https://www.hal.inserm.fr/inserm-03867929
Submitted on : Wednesday, November 23, 2022-3:37:02 PM
Last modification on : Saturday, November 26, 2022-8:31:19 AM
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- HAL Id : inserm-03867929 , version 1
- DOI : 10.1111/cge.13062
- PUBMED : 28762477
Cite
A. Lavillaureix, S. Heide, S. Chantot-Bastaraud, I. Marey, B. Keren, et al.. Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly. Clinical Genetics, 2017, 92 (5), pp.556-558. ⟨10.1111/cge.13062⟩. ⟨inserm-03867929⟩
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