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Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients.
Clin Genet. 2018 Mar;93(3):567-576. doi: 10.1111/cge.13102. Epub 2017 Oct 4.
Clin Genet. 2018.
PMID: 28708303
Free article.
Karyotype is not dead (yet)!
Pasquier L, Fradin M, Chérot E, Martin-Coignard D, Colin E, Journel H, Demurger F, Akloul L, Quélin C, Jauffret V, Lucas J, Belaud-Rotureau MA, Odent S, Jaillard S.
Pasquier L, et al. Among authors: cherot e.
Eur J Med Genet. 2016 Jan;59(1):11-5. doi: 10.1016/j.ejmg.2015.11.016. Epub 2015 Dec 10.
Eur J Med Genet. 2016.
PMID: 26691665
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De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.
Küry S, van Woerden GM, Besnard T, Proietti Onori M, Latypova X, Towne MC, Cho MT, Prescott TE, Ploeg MA, Sanders S, Stessman HAF, Pujol A, Distel B, Robak LA, Bernstein JA, Denommé-Pichon AS, Lesca G, Sellars EA, Berg J, Carré W, Busk ØL, van Bon BWM, Waugh JL, Deardorff M, Hoganson GE, Bosanko KB, Johnson DS, Dabir T, Holla ØL, Sarkar A, Tveten K, de Bellescize J, Braathen GJ, Terhal PA, Grange DK, van Haeringen A, Lam C, Mirzaa G, Burton J, Bhoj EJ, Douglas J, Santani AB, Nesbitt AI, Helbig KL, Andrews MV, Begtrup A, Tang S, van Gassen KLI, Juusola J, Foss K, Enns GM, Moog U, Hinderhofer K, Paramasivam N, Lincoln S, Kusako BH, Lindenbaum P, Charpentier E, Nowak CB, Cherot E, Simonet T, Ruivenkamp CAL, Hahn S, Brownstein CA, Xia F, Schmitt S, Deb W, Bonneau D, Nizon M, Quinquis D, Chelly J, Rudolf G, Sanlaville D, Parent P, Gilbert-Dussardier B, Toutain A, Sutton VR, Thies J, Peart-Vissers LELM, Boisseau P, Vincent M, Grabrucker AM, Dubourg C; Undiagnosed Diseases Network; Tan WH, Verbeek NE, Granzow M, Santen GWE, Shendure J, Isidor B, Pasquier L, Redon R, Yang Y, State MW, Kleefstra T, Cogné B; GEM HUGO; Deciphering Developmental Disorders Study; Petrovski S, Retterer K…
See abstract for full author list ➔
Küry S, et al. Among authors: cherot e.
Am J Hum Genet. 2017 Nov 2;101(5):768-788. doi: 10.1016/j.ajhg.2017.10.003.
Am J Hum Genet. 2017.
PMID: 29100089
Free PMC article.
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Significance of echogenic foci in the left ventricle of the fetal heart in a low-risk population.
Jaffe R, Cherot E, Allen T, Glantz JC.
Jaffe R, et al. Among authors: cherot e.
Fetal Diagn Ther. 1999 Nov-Dec;14(6):345-7. doi: 10.1159/000020955.
Fetal Diagn Ther. 1999.
PMID: 10640873
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Impact of vitamin A supplementation on the incidence of infection in elderly nursing-home residents: a randomized controlled trial.
Murphy S, West KP Jr, Greenough WB 3rd, Cherot E, Katz J, Clement L.
Murphy S, et al. Among authors: cherot e.
Age Ageing. 1992 Nov;21(6):435-9. doi: 10.1093/ageing/21.6.435.
Age Ageing. 1992.
PMID: 1471582
Clinical Trial.
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Measurement of knee height in frail, elderly nursing home residents.
Murphy S, Cherot EK, Clement L, West KP Jr.
Murphy S, et al. Among authors: cherot ek.
Am J Clin Nutr. 1991 Sep;54(3):611-2. doi: 10.1093/ajcn/54.3.611.
Am J Clin Nutr. 1991.
PMID: 1877523
No abstract available.
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