Doray B - Search Results

1

Recurrent neural tube defects associated with partial trisomy 2p22-pter: report of two siblings and review of the literature.

Doray B, Favre R, Gasser B, Girard-Lemaire F, Schluth C, Flori E. Doray B, et al. Genet Couns. 2003;14(2):165-72. Genet Couns. 2003. PMID: 12872810 Review.

2

Prenatal diagnosis of a true fetal tetraploidy in direct and cultured chorionic villi.

Schluth C, Doray B, Girard-Lemaire F, Favre R, Flori J, Gasser B, Rudolf G, Flori E. Schluth C, et al. Among authors: doray b. Genet Couns. 2004;15(4):429-36. Genet Couns. 2004. PMID: 15658618

3

Prenatal sonographic diagnosis of the 49,XXXXY syndrome.

Schluth C, Doray B, Girard-Lemaire F, Kohler M, Langer B, Gasser B, Lindner V, Flori E. Schluth C, et al. Among authors: doray b. Prenat Diagn. 2002 Dec;22(13):1177-80. doi: 10.1002/pd.473. Prenat Diagn. 2002. PMID: 12478628 Review.

4

Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader-Willi and Angelman syndromes.

Flori E, Biancalana V, Girard-Lemaire F, Favre R, Flori J, Doray B, Mandel JL. Flori E, et al. Among authors: doray b. Eur J Hum Genet. 2004 Mar;12(3):181-6. doi: 10.1038/sj.ejhg.5201134. Eur J Hum Genet. 2004. PMID: 14694357

5

Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndrome.

Flori E, Girodon E, Samama B, Becmeur F, Viville B, Girard-Lemaire F, Doray B, Schluth C, Marcellin L, Boehm N, Goossens M, Pingault V. Flori E, et al. Among authors: doray b. Eur J Hum Genet. 2005 Sep;13(9):1013-8. doi: 10.1038/sj.ejhg.5201442. Eur J Hum Genet. 2005. PMID: 15915162

6

Neural tube defects: the experience of the registry of congenital malformations of Alsace, France, 1995-2009.

Timbolschi D, Schaefer E, Monga B, Fattori D, Dott B, Favre R, Kohler M, Nisand I, Viville B, Astruc D, Kehrli P, Gasser B, Lindner V, Marcellin L, Flori E, Girard-Lemaire F, Dollfus H, Doray B. Timbolschi D, et al. Among authors: doray b. Fetal Diagn Ther. 2015;37(1):6-17. doi: 10.1159/000362663. Epub 2014 Nov 11. Fetal Diagn Ther. 2015. PMID: 25402326 Free article.

7

Pallister-Killian syndrome: difficulties of prenatal diagnosis.

Doray B, Girard-Lemaire F, Gasser B, Baldauf JJ, De Geeter B, Spizzo M, Zeidan C, Flori E. Doray B, et al. Prenat Diagn. 2002 Jun;22(6):470-7. doi: 10.1002/pd.342. Prenat Diagn. 2002. PMID: 12116305

8

Hereditary renal adysplasia in a three generations family.

Doray B, Gasser B, Reinartz I, Stoll C. Doray B, et al. Genet Couns. 1999;10(3):251-7. Genet Couns. 1999. PMID: 10546096

9

[Epidemiology of orofacial clefts (1995-2006) in France (Congenital Malformations of Alsace Registry)].

Doray B, Badila-Timbolschi D, Schaefer E, Fattori D, Monga B, Dott B, Favre R, Kohler M, Nisand I, Viville B, Kauffmann I, Bruant-Rodier C, Grollemund B, Rinkenbach R, Astruc D, Gasser B, Lindner V, Marcellin L, Flori E, Girard-Lemaire F, Dollfus H. Doray B, et al. Arch Pediatr. 2012 Oct;19(10):1021-9. doi: 10.1016/j.arcped.2012.07.002. Epub 2012 Aug 24. Arch Pediatr. 2012. PMID: 22925539 French.

10

Mosaic trisomy 13 on chorionic villi in a fetus with body wall complex: fortuitous association or pathogenic hypothesis?

Doray B, Viville B, Touret Y, Gasser B, Samama B, Boehm N, Girard-Lemaire F, Schluth C, Flori E. Doray B, et al. Prenat Diagn. 2003 Dec 15;23(12):1021-3. doi: 10.1002/pd.730. Prenat Diagn. 2003. PMID: 14663843 No abstract available.

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