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Fetal RhD genotyping by maternal serum analysis: a two-year experience.
Am J Obstet Gynecol. 2005 Mar;192(3):666-9. doi: 10.1016/j.ajog.2004.10.632.
Am J Obstet Gynecol. 2005.
PMID: 15746656
Chimeric LNA/DNA probes as a detection system for real-time PCR.
Costa JM, Ernault P, Olivi M, Gaillon T, Arar K.
Costa JM, et al. Among authors: gaillon t.
Clin Biochem. 2004 Oct;37(10):930-2. doi: 10.1016/j.clinbiochem.2004.05.020.
Clin Biochem. 2004.
PMID: 15369726
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Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders.
El Khouri E, Ghoumid J, Haye D, Giuliano F, Drevillon L, Briand-Suleau A, De La Grange P, Nau V, Gaillon T, Bienvenu T, Jacquemin-Sablon H, Goossens M, Amselem S, Giurgea I.
El Khouri E, et al. Among authors: gaillon t.
Mol Psychiatry. 2021 Jul;26(7):3572-3585. doi: 10.1038/s41380-021-01072-7. Epub 2021 Apr 19.
Mol Psychiatry. 2021.
PMID: 33867523
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Novel comprehensive diagnostic strategy in Pitt-Hopkins syndrome: clinical score and further delineation of the TCF4 mutational spectrum.
Whalen S, Héron D, Gaillon T, Moldovan O, Rossi M, Devillard F, Giuliano F, Soares G, Mathieu-Dramard M, Afenjar A, Charles P, Mignot C, Burglen L, Van Maldergem L, Piard J, Aftimos S, Mancini G, Dias P, Philip N, Goldenberg A, Le Merrer M, Rio M, Josifova D, Van Hagen JM, Lacombe D, Edery P, Dupuis-Girod S, Putoux A, Sanlaville D, Fischer R, Drévillon L, Briand-Suleau A, Metay C, Goossens M, Amiel J, Jacquette A, Giurgea I.
Whalen S, et al. Among authors: gaillon t.
Hum Mutat. 2012 Jan;33(1):64-72. doi: 10.1002/humu.21639. Epub 2011 Nov 23.
Hum Mutat. 2012.
PMID: 22045651
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TCF4 deletions in Pitt-Hopkins Syndrome.
Giurgea I, Missirian C, Cacciagli P, Whalen S, Fredriksen T, Gaillon T, Rankin J, Mathieu-Dramard M, Morin G, Martin-Coignard D, Dubourg C, Chabrol B, Arfi J, Giuliano F, Claude Lambert J, Philip N, Sarda P, Villard L, Goossens M, Moncla A.
Giurgea I, et al. Among authors: gaillon t.
Hum Mutat. 2008 Nov;29(11):E242-51. doi: 10.1002/humu.20859.
Hum Mutat. 2008.
PMID: 18781613
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