Soupre V - Search Results

1

Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome.

Gaston V, Le Bouc Y, Soupre V, Vazquez MP, Gicquel C. Gaston V, et al. Among authors: soupre v. Horm Res. 2000;54(1):1-5. doi: 10.1159/000063429. Horm Res. 2000. PMID: 11182628

2

Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait.

Houdayer C, Soupre V, Rosenberg-Bourgin M, Martinez H, Tredano M, Feldmann D, Feingold J, Aymard P, Munnich A, Le Bouc Y, Vazquez MP, Bahuau M. Houdayer C, et al. Among authors: soupre v. Ann Genet. 1999;42(2):69-74. Ann Genet. 1999. PMID: 10434119

3

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.

Gaston V, Le Bouc Y, Soupre V, Burglen L, Donadieu J, Oro H, Audry G, Vazquez MP, Gicquel C. Gaston V, et al. Among authors: soupre v. Eur J Hum Genet. 2001 Jun;9(6):409-18. doi: 10.1038/sj.ejhg.5200649. Eur J Hum Genet. 2001. PMID: 11436121

4

Pierre Robin sequence and interstitial deletion 2q32.3-q33.2.

Houdayer C, Portnoï MF, Vialard F, Soupre V, Crumière C, Taillemite JL, Couderc R, Vazquez MP, Bahuau M. Houdayer C, et al. Among authors: soupre v. Am J Med Genet. 2001 Aug 15;102(3):219-26. doi: 10.1002/ajmg.1448. Am J Med Genet. 2001. PMID: 11484197

5

FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate.

Bahuau M, Houdayer C, Tredano M, Soupre V, Couderc R, Vazquez MP. Bahuau M, et al. Among authors: soupre v. Clin Genet. 2002 Dec;62(6):470-3. doi: 10.1034/j.1399-0004.2002.620608.x. Clin Genet. 2002. PMID: 12485195

6

Craniofacial phenotype in the branchio-oculo-facial syndrome: four case reports.

Galliani E, Burglen L, Kadlub N, Just W, Sznajer Y, de Villemeur TB, Soupre V, Picard A, Vazquez MP. Galliani E, et al. Among authors: soupre v. Cleft Palate Craniofac J. 2012 May;49(3):357-64. doi: 10.1597/10-203. Epub 2011 May 3. Cleft Palate Craniofac J. 2012. PMID: 21539471

7

[Wiedemann-Beckwith syndrome: a new approach for reduction glossoplasty using Ultracision(®)].

Dutot MC, Soupre V, Vazquez MP, Picard A, Kadlub N. Dutot MC, et al. Among authors: soupre v. Rev Stomatol Chir Maxillofac Chir Orale. 2015 Apr;116(2):82-5. doi: 10.1016/j.revsto.2014.11.008. Epub 2015 Jan 9. Rev Stomatol Chir Maxillofac Chir Orale. 2015. PMID: 25582551 French.

8

Speech outcome after intravelar veloplasty.

Moreau A, Charpuis-Vandenbogaerde C, Neiva-Vaz C, Sanquer E, Soupre V, Vazquez MP, Picard A, Kadlub N. Moreau A, et al. Among authors: soupre v. J Stomatol Oral Maxillofac Surg. 2021 Apr;122(2):147-150. doi: 10.1016/j.jormas.2020.05.015. Epub 2020 May 23. J Stomatol Oral Maxillofac Surg. 2021. PMID: 32450319

9

[Circumscribed mandibular osteitis in children due to hematogenous dissemination. Apropos of 5 clinical cases].

Franchi G, Soupre V, Karcenty B, Buis J, Diner PA, Vazquez MP. Franchi G, et al. Among authors: soupre v. Rev Stomatol Chir Maxillofac. 1999 May;100(2):70-4. Rev Stomatol Chir Maxillofac. 1999. PMID: 10488488 French.

10

1q32-q41 microdeletion with reference to Van der Woude syndrome and allied clefting entities.

Houdayer C, Soupre V, Karcenty B, Vazquez MP, Odent S, Lacombe D, Le Bouc Y, Munnich A, Bahuau M. Houdayer C, et al. Among authors: soupre v. Am J Med Genet. 2000 Mar 13;91(2):161-3. doi: 10.1002/(sici)1096-8628(20000313)91:2<161::aid-ajmg18>3.0.co;2-q. Am J Med Genet. 2000. PMID: 10748420 No abstract available.

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