Brisset S - Search Results

1

A CGH study of 27 patients with CHARGE association.

Sanlaville D, Romana SP, Lapierre JM, Amiel J, Genevieve D, Ozilou C, Le Lorch M, Brisset S, Gosset P, Baumann C, Turleau C, Lyonnet S, Vekemans M. Sanlaville D, et al. Among authors: brisset s. Clin Genet. 2002 Feb;61(2):135-8. doi: 10.1034/j.1399-0004.2002.610208.x. Clin Genet. 2002. PMID: 11940088

2

Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.

Brisset S, Joly G, Ozilou C, Lapierre JM, Gosset P, LeLorc'h M, Raoul O, Turleau C, Vekemans M, Romana SP. Brisset S, et al. Am J Med Genet. 2002 Dec 15;113(4):339-45. doi: 10.1002/ajmg.b.10740. Am J Med Genet. 2002. PMID: 12457405 Review.

3

[Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities].

Romana SP, Gosset P, Elghezal H, Le Lorc'h M, Ozilou C, Lapierre JM, Sanlaville D, Brisset S, Turleau C, Vekemans M. Romana SP, et al. Among authors: brisset s. J Gynecol Obstet Biol Reprod (Paris). 2001 Feb;30(1 Suppl):75-9. J Gynecol Obstet Biol Reprod (Paris). 2001. PMID: 11240520 Free article. Review. French. No abstract available.

4

Molecular cytogenetic characterization of a 4p15.1-pter duplication and a 4q35.1-qter deletion in a recombinant of chromosome 4 pericentric inversion.

Maurin ML, Labrune P, Brisset S, Le Lorc'h M, Pineau D, Castel C, Romana S, Tachdjian G. Maurin ML, et al. Among authors: brisset s. Am J Med Genet A. 2009 Feb;149A(2):226-31. doi: 10.1002/ajmg.a.32603. Am J Med Genet A. 2009. PMID: 19161154 Review.

5

CGH analysis in a cohort of 17 chromosomally normal fetuses with an increased nuchal translucency.

Brisset S, Romana S, Texier I, Lapierre JM, North MO, Vekemans M, Morichon-Delvallez N. Brisset S, et al. Prenat Diagn. 2003 Dec 15;23(12):1017-8. doi: 10.1002/pd.677. Prenat Diagn. 2003. PMID: 14663841 No abstract available.

6

Chromosomal translocations and semen quality: A study on 144 male translocation carriers.

Mayeur A, Ahdad N, Hesters L, Brisset S, Romana S, Tosca L, Tachdjian G, Frydman N. Mayeur A, et al. Among authors: brisset s. Reprod Biomed Online. 2019 Jan;38(1):46-55. doi: 10.1016/j.rbmo.2018.10.003. Epub 2018 Nov 13. Reprod Biomed Online. 2019. PMID: 30518499

7

Terminal 14q32.33 deletion: genotype-phenotype correlation.

Maurin ML, Brisset S, Le Lorc'h M, Poncet V, Trioche P, Aboura A, Labrune P, Tachdjian G. Maurin ML, et al. Among authors: brisset s. Am J Med Genet A. 2006 Nov 1;140(21):2324-9. doi: 10.1002/ajmg.a.31438. Am J Med Genet A. 2006. PMID: 17022077 Review.

8

First prenatal case of proximal 19p13.12 microdeletion syndrome: New insights and new delineation of the syndrome.

Huynh MT, Tosca L, Petit F, Martinovic J, Proust A, Bouligand J, Amiel J, Azria E, Parisot F, Benoit V, Receveur A, Drévillon L, Tachdjian G, Brisset S. Huynh MT, et al. Among authors: brisset s. Eur J Med Genet. 2018 Jun;61(6):322-328. doi: 10.1016/j.ejmg.2018.01.009. Epub 2018 Feb 3. Eur J Med Genet. 2018. PMID: 29366875

9

SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplication.

Briand-Suleau A, Martinovic J, Tosca L, Tou B, Brisset S, Bouligand J, Delattre V, Giurgea I, Bachir J, Folliot P, Goumy C, Francannet C, Guiochon-Mantel A, Benachi A, Vermeesch J, Tachdjian G, Vago P, Goossens M, Métay C. Briand-Suleau A, et al. Among authors: brisset s. Eur J Med Genet. 2014 Mar;57(4):174-80. doi: 10.1016/j.ejmg.2013.12.013. Epub 2014 Jan 29. Eur J Med Genet. 2014. PMID: 24486774 Free article.

10

CGH analysis of secondary genetic changes in Ewing tumors: correlation with metastatic disease in a series of 43 cases.

Brisset S, Schleiermacher G, Peter M, Mairal A, Oberlin O, Delattre O, Aurias A. Brisset S, et al. Cancer Genet Cytogenet. 2001 Oct 1;130(1):57-61. doi: 10.1016/s0165-4608(01)00454-x. Cancer Genet Cytogenet. 2001. PMID: 11672775 Review.

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