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Page 1
Binder phenotype: clinical and etiological heterogeneity of the so-called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature.
Levaillant JM, Moeglin D, Zouiten K, Bucourt M, Burglen L, Soupre V, Baumann C, Jaquemont ML, Touraine R, Picard A, Vuillard E, Belarbi N, Oury JF, Verloes A, Vazquez MP, Labrune P, Delezoide AL, Gérard-Blanluet M. Levaillant JM, et al. Among authors: bucourt m. Prenat Diagn. 2009 Feb;29(2):140-50. doi: 10.1002/pd.2167. Prenat Diagn. 2009. PMID: 19156647
Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 cases.
Tessier A, Sarreau M, Pelluard F, André G, Blesson S, Bucourt M, Dechelotte P, Faivre L, Frébourg T, Goldenberg A, Goua V, Jeanne-Pasquier C, Guimiot F, Laquerriere A, Laurent N, Lefebvre M, Loget P, Maréchaud M, Mechler C, Perez MJ, Sabourin JC, Verloes A, Patrier S, Guerrot AM. Tessier A, et al. Among authors: bucourt m. Prenat Diagn. 2016 Dec;36(13):1270-1275. doi: 10.1002/pd.4971. Epub 2016 Dec 9. Prenat Diagn. 2016. PMID: 27859469 Review.
Ultrasound assessment in a case of sialic acid storage disease.
Carbillon L, Largillière C, Bucourt M, Scheuer-Niro B, Levaillant JM, Uzan M. Carbillon L, et al. Among authors: bucourt m. Ultrasound Obstet Gynecol. 2001 Sep;18(3):272-4. doi: 10.1046/j.0960-7692.2001.00515.x. Ultrasound Obstet Gynecol. 2001. PMID: 11555460 Free article.
Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases.
Adle-Biassette H, Saugier-Veber P, Fallet-Bianco C, Delezoide AL, Razavi F, Drouot N, Bazin A, Beaufrère AM, Bessières B, Blesson S, Bucourt M, Carles D, Devisme L, Dijoud F, Fabre B, Fernandez C, Gaillard D, Gonzales M, Jossic F, Joubert M, Laurent N, Leroy B, Loeuillet L, Loget P, Marcorelles P, Martinovic J, Perez MJ, Satge D, Sinico M, Tosi M, Benichou J, Gressens P, Frebourg T, Laquerrière A. Adle-Biassette H, et al. Among authors: bucourt m. Acta Neuropathol. 2013 Sep;126(3):427-42. doi: 10.1007/s00401-013-1146-1. Epub 2013 Jul 3. Acta Neuropathol. 2013. PMID: 23820807
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Laquerriere A, Jaber D, Abiusi E, Maluenda J, Mejlachowicz D, Vivanti A, Dieterich K, Stoeva R, Quevarec L, Nolent F, Biancalana V, Latour P, Sternberg D, Capri Y, Verloes A, Bessieres B, Loeuillet L, Attie-Bitach T, Martinovic J, Blesson S, Petit F, Beneteau C, Whalen S, Marguet F, Bouligand J, Héron D, Viot G, Amiel J, Amram D, Bellesme C, Bucourt M, Faivre L, Jouk PS, Khung S, Sigaudy S, Delezoide AL, Goldenberg A, Jacquemont ML, Lambert L, Layet V, Lyonnet S, Munnich A, Van Maldergem L, Piard J, Guimiot F, Landrieu P, Letard P, Pelluard F, Perrin L, Saint-Frison MH, Topaloglu H, Trestard L, Vincent-Delorme C, Amthor H, Barnerias C, Benachi A, Bieth E, Boucher E, Cormier-Daire V, Delahaye-Duriez A, Desguerre I, Eymard B, Francannet C, Grotto S, Lacombe D, Laffargue F, Legendre M, Martin-Coignard D, Mégarbané A, Mercier S, Nizon M, Rigonnot L, Prieur F, Quélin C, Ranjatoelina-Randrianaivo H, Resta N, Toutain A, Verhelst H, Vincent M, Colin E, Fallet-Bianco C, Granier M, Grigorescu R, Saada J, Gonzales M, Guiochon-Mantel A, Bessereau JL, Tawk M, Gut I, Gitiaux C, Melki J. Laquerriere A, et al. Among authors: bucourt m. J Med Genet. 2022 Jun;59(6):559-567. doi: 10.1136/jmedgenet-2020-107595. Epub 2021 Apr 5. J Med Genet. 2022. PMID: 33820833 Free PMC article.
Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutations.
Legendre M, Gonzales M, Goudefroye G, Bilan F, Parisot P, Perez MJ, Bonnière M, Bessières B, Martinovic J, Delezoide AL, Jossic F, Fallet-Bianco C, Bucourt M, Tantau J, Loget P, Loeuillet L, Laurent N, Leroy B, Salhi H, Bigi N, Rouleau C, Guimiot F, Quélin C, Bazin A, Alby C, Ichkou A, Gesny R, Kitzis A, Ville Y, Lyonnet S, Razavi F, Gilbert-Dussardier B, Vekemans M, Attié-Bitach T. Legendre M, et al. Among authors: bucourt m. J Med Genet. 2012 Nov;49(11):698-707. doi: 10.1136/jmedgenet-2012-100926. Epub 2012 Sep 28. J Med Genet. 2012. PMID: 23024289
Prenatal assessment of a fast-growing giant epignathus.
Faghfouri F, Bucourt M, Garel C, Benchimol M, Amarenco B, Soupre V, Benbara A, Carbillon L. Faghfouri F, et al. Among authors: bucourt m. Fetal Pediatr Pathol. 2014 Feb;33(1):55-9. doi: 10.3109/15513815.2013.850134. Epub 2013 Oct 28. Fetal Pediatr Pathol. 2014. PMID: 24164281
Structural chromosomal mosaicism and prenatal diagnosis.
Pipiras E, Dupont C, Chantot-Bastaraud S, Siffroi JP, Bucourt M, Batallan A, Largillière C, Uzan M, Wolf JP, Benzacken B. Pipiras E, et al. Among authors: bucourt m. Prenat Diagn. 2004 Feb;24(2):101-3. doi: 10.1002/pd.797. Prenat Diagn. 2004. PMID: 14974115
Prenatal diagnosis of Roberts syndrome: two new cases.
Benzacken B, Savary JB, Manouvrier S, Bucourt M, Gonzales J. Benzacken B, et al. Among authors: bucourt m. Prenat Diagn. 1996 Feb;16(2):125-30. doi: 10.1002/(SICI)1097-0223(199602)16:2<125::AID-PD822>3.0.CO;2-S. Prenat Diagn. 1996. PMID: 8650122
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