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Exome sequencing identifies the first genetic determinants of sirenomelia in humans.
Lecoquierre F, Brehin AC, Coutant S, Coursimault J, Bazin A, Finck W, Benoist G, Begorre M, Beneteau C, Cailliez D, Chenal P, De Jong M, Degré S, Devisme L, Francannet C, Gérard B, Jeanne C, Joubert M, Journel H, Laurichesse Delmas H, Layet V, Liquier A, Mangione R, Patrier S, Pelluard F, Petit F, Tillouche N, van Ravenswaaij-Arts C, Frebourg T, Saugier-Veber P, Gruchy N, Nicolas G, Gerard M. Lecoquierre F, et al. Among authors: begorre m. Hum Mutat. 2020 May;41(5):926-933. doi: 10.1002/humu.23998. Epub 2020 Mar 1. Hum Mutat. 2020. PMID: 32058622
12q21 Microdeletion in a fetus with Meckel syndrome involving CEP290/MKS4.
Molin A, Benoist G, Jeanne-Pasquier C, Elkartoufi N, Litzer J, Decamp M, Gruchy N, Durand-Malbruny M, Begorre M, Attie-Bitach T, Leporrier N. Molin A, et al. Among authors: begorre m. Eur J Med Genet. 2013 Oct;56(10):580-3. doi: 10.1016/j.ejmg.2013.08.002. Epub 2013 Aug 15. Eur J Med Genet. 2013. PMID: 23954617
First-trimester prenatal diagnosis performed on pregnant women with fetal ultrasound abnormalities: the reliability of interphase fluorescence in situ hybridization (FISH) on mesenchymal core for the main aneuploidies.
Toutain J, Epiney M, Begorre M, Dessuant H, Vandenbossche F, Horovitz J, Saura R. Toutain J, et al. Among authors: begorre m. Eur J Obstet Gynecol Reprod Biol. 2010 Apr;149(2):143-6. doi: 10.1016/j.ejogrb.2009.12.015. Epub 2010 Jan 4. Eur J Obstet Gynecol Reprod Biol. 2010. PMID: 20045588
Cation exchange versus multimodal cation exchange resins for antibody capture from CHO supernatants: identification of contaminating host cell proteins by mass spectrometry.
Joucla G, Le Sénéchal C, Bégorre M, Garbay B, Santarelli X, Cabanne C. Joucla G, et al. Among authors: begorre m. J Chromatogr B Analyt Technol Biomed Life Sci. 2013 Dec 30;942-943:126-33. doi: 10.1016/j.jchromb.2013.10.033. Epub 2013 Oct 25. J Chromatogr B Analyt Technol Biomed Life Sci. 2013. PMID: 24239937
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