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You searched for: Author/Creator Le Goff, Carine

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1. Hypoalphalipoproteinemia and BRAFV600E Mutation Are Major Predictors of Aortic Infiltration in the Erdheim-Chester Disease. Issue 8 (August 2018)

3. Molecular screening of ADAMTSL2 gene in 33 patients reveals the genetic heterogeneity of geleophysic dysplasia. Issue 6 (17th March 2011)

4. Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasia. Issue 7 (11th April 2016)

7. The critical role of the TB5 domain of fibrillin-1 in endochondral ossification. Issue 22 (4th June 2022)