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Usefulness of fluorescence in situ hybridization for the diagnosis of Turner mosaic fetuses with small ring X chromosomes.
Siffroi JP, Dupuy O, Joye N, Le Bourhis C, Benzacken B, Portnoi M, Berkane N, Franco JC, Studer C, Carbonne B, Gonzales M, Bucourt M, Uzan S, Uzan M, Milliez J, Wolf JP, Taillemite J, Dadoune JP. Siffroi JP, et al. Among authors: bucourt m. Fetal Diagn Ther. 2000 Jul-Aug;15(4):229-33. doi: 10.1159/000021012. Fetal Diagn Ther. 2000. PMID: 10867485
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
First-trimester diagnosis of sirenomelia. A case report.
Carbillon L, Seince N, Largillière C, Bucourt M, Uzan M. Carbillon L, et al. Among authors: bucourt m. Fetal Diagn Ther. 2001 Sep-Oct;16(5):284-8. doi: 10.1159/000053929. Fetal Diagn Ther. 2001. PMID: 11509850 Review.
Semilobar holoprosencephaly prenatal diagnosis: an unexpected complex rearrangement in a de novo apparently balanced reciprocal translocation on karyotype.
Kanafani S, Aboura A, Pipiras E, Carbillon L, Tabet AC, Largillière C, Garel C, Gressens P, Bucourt M, Cedrin-Durnerin I, Lachassinne E, Roumegoux C, Uzan M, Hugues JN, Wolf JP, Benzacken B. Kanafani S, et al. Among authors: bucourt m. Prenat Diagn. 2007 Mar;27(3):279-84. doi: 10.1002/pd.1639. Prenat Diagn. 2007. PMID: 17269127
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.
3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.
Dupont C, Bucourt M, Guimiot F, Kraoua L, Smiljkovski D, Le Tessier D, Lebugle C, Gerard B, Spaggiari E, Bourdoncle P, Tabet AC, Benzacken B, Dupont JM. Dupont C, et al. Among authors: bucourt m. Mol Cytogenet. 2014 Sep 30;7(1):59. doi: 10.1186/s13039-014-0059-6. eCollection 2014. Mol Cytogenet. 2014. PMID: 25320640 Free PMC article.
110 results