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Genetic homogeneity of the Camurati-Engelmann disease.
Belinda A, Xavier CF, Saraiva JM, Le Merrer M, Dagoneau N, Huber C, Penet C, Munnich A, Cormier-Daire V. Belinda A, et al. Among authors: huber c. Clin Genet. 2000 Aug;58(2):150-2. doi: 10.1034/j.1399-0004.2000.580211.x. Clin Genet. 2000. PMID: 11005150 No abstract available.
Sulphate transporter gene mutations in apparently isolated club foot.
Huber C, Odent S, Rumeur S, Padovani P, Penet C, Cormier-Daire V, Munnich A, Le Merrer M. Huber C, et al. J Med Genet. 2001 Mar;38(3):191-3. doi: 10.1136/jmg.38.3.191. J Med Genet. 2001. PMID: 11303514 Free PMC article. No abstract available.
SHOX point mutations in dyschondrosteosis.
Huber C, Cusin V, Le Merrer M, Mathieu M, Sulmont V, Dagoneau N, Munnich A, Cormier-Daire V. Huber C, et al. J Med Genet. 2001 May;38(5):323. doi: 10.1136/jmg.38.5.323. J Med Genet. 2001. PMID: 11403039 Free PMC article. No abstract available.
[Genetics and the SHOX gene].
Huber C, Cormier-Daire V. Huber C, et al. Arch Pediatr. 2004 Jun;11(6):555-6. doi: 10.1016/j.arcped.2004.03.057. Arch Pediatr. 2004. PMID: 15158831 French. No abstract available.
ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndrome.
Dagoneau N, Benoist-Lasselin C, Huber C, Faivre L, Mégarbané A, Alswaid A, Dollfus H, Alembik Y, Munnich A, Legeai-Mallet L, Cormier-Daire V. Dagoneau N, et al. Among authors: huber c. Am J Hum Genet. 2004 Nov;75(5):801-6. doi: 10.1086/425231. Epub 2004 Sep 13. Am J Hum Genet. 2004. PMID: 15368195 Free PMC article.
1,864 results