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Novel comprehensive diagnostic strategy in Pitt-Hopkins syndrome: clinical score and further delineation of the TCF4 mutational spectrum.
Hum Mutat. 2012 Jan;33(1):64-72. doi: 10.1002/humu.21639. Epub 2011 Nov 23.
Hum Mutat. 2012.
PMID: 22045651
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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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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Fetal RhD genotyping by maternal serum analysis: a two-year experience.
Gautier E, Benachi A, Giovangrandi Y, Ernault P, Olivi M, Gaillon T, Costa JM.
Gautier E, et al. Among authors: gaillon t.
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
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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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