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Page 1
Twelve new patients with 13q deletion syndrome: genotype-phenotype analyses in progress.
Quélin C, Bendavid C, Dubourg C, de la Rochebrochard C, Lucas J, Henry C, Jaillard S, Loget P, Loeuillet L, Lacombe D, Rival JM, David V, Odent S, Pasquier L. Quélin C, et al. Among authors: de la rochebrochard c. Eur J Med Genet. 2009 Jan-Feb;52(1):41-6. doi: 10.1016/j.ejmg.2008.10.002. Epub 2008 Oct 31. Eur J Med Genet. 2009. PMID: 19022413
Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases.
Pasquier L, Marcorelles P, Loget P, Pelluard F, Carles D, Perez MJ, Bendavid C, de La Rochebrochard C, Ferry M, David V, Odent S, Laquerrière A. Pasquier L, et al. Among authors: de la rochebrochard c. Acta Neuropathol. 2009 Feb;117(2):185-200. doi: 10.1007/s00401-008-0469-9. Epub 2008 Dec 5. Acta Neuropathol. 2009. PMID: 19057916
[Syndromic mental retardation].
Odent S, Pasquier L, de la Rochebrochard C, Journel H, Lazaro L. Odent S, et al. Among authors: de la rochebrochard c. Arch Pediatr. 2008 Jun;15(5):705-7. doi: 10.1016/S0929-693X(08)71882-7. Arch Pediatr. 2008. PMID: 18582721 French. No abstract available.
Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation.
Saugier-Veber P, Goldenberg A, Drouin-Garraud V, de La Rochebrochard C, Layet V, Drouot N, Le Meur N, Gilbert-Du-Ssardier B, Joly-Hélas G, Moirot H, Rossi A, Tosi M, Frébourg T. Saugier-Veber P, et al. Among authors: de la rochebrochard c. Eur J Hum Genet. 2006 Sep;14(9):1009-17. doi: 10.1038/sj.ejhg.5201661. Epub 2006 Jun 14. Eur J Hum Genet. 2006. PMID: 16773131
The intrafamilial variability of the 22q11.2 microduplication encompasses a spectrum from minor cognitive deficits to severe congenital anomalies.
de La Rochebrochard C, Joly-Hélas G, Goldenberg A, Durand I, Laquerrière A, Ickowicz V, Saugier-Veber P, Eurin D, Moirot H, Diguet A, de Kergal F, Tiercin C, Mace B, Marpeau L, Frebourg T. de La Rochebrochard C, et al. Am J Med Genet A. 2006 Jul 15;140(14):1608-13. doi: 10.1002/ajmg.a.31227. Am J Med Genet A. 2006. PMID: 16761289 No abstract available.