Doray B - Search Results

1

Esophageal and duodenal atresia in a girl with a 12q24.3-qter deletion.

Doray B, Becmeur F, Girard-Lemaire F, Schluth C, Flori E. Doray B, et al. Clin Genet. 2002 Jun;61(6):468-71. doi: 10.1034/j.1399-0004.2002.610613.x. Clin Genet. 2002. PMID: 12121357 No abstract available.

2

Failure of prenatal diagnosis of diploid-triploid mosaicism after amniocentesis.

Flori E, Doray B, Rudolf G, Favre R, Girard-Lemaire F, Schluth C, Zix-Kieffer I, Flori J, Loriot M, Schmitt E, Rumpler Y. Flori E, et al. Among authors: doray b. Clin Genet. 2003 Apr;63(4):328-31. doi: 10.1034/j.1399-0004.2003.00062.x. Clin Genet. 2003. PMID: 12702170 No abstract available.

3

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

4

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

5

Delineation of 15q13.3 microdeletions.

Masurel-Paulet A, Andrieux J, Callier P, Cuisset JM, Le Caignec C, Holder M, Thauvin-Robinet C, Doray B, Flori E, Alex-Cordier MP, Beri M, Boute O, Delobel B, Dieux A, Vallee L, Jaillard S, Odent S, Isidor B, Beneteau C, Vigneron J, Bilan F, Gilbert-Dussardier B, Dubourg C, Labalme A, Bidon C, Gautier A, Pernes P, Pinoit JM, Huet F, Mugneret F, Aral B, Jonveaux P, Sanlaville D, Faivre L. Masurel-Paulet A, et al. Among authors: doray b. Clin Genet. 2010 Aug;78(2):149-61. doi: 10.1111/j.1399-0004.2010.01374.x. Epub 2010 Feb 9. Clin Genet. 2010. PMID: 20236110

6

Osteosclerotic bone dysplasia in siblings with a Fam20C mutation.

Fradin M, Stoetzel C, Muller J, Koob M, Christmann D, Debry C, Kohler M, Isnard M, Astruc D, Desprez P, Zorres C, Flori E, Dollfus H, Doray B. Fradin M, et al. Among authors: doray b. Clin Genet. 2011 Aug;80(2):177-83. doi: 10.1111/j.1399-0004.2010.01516.x. Epub 2010 Jul 23. Clin Genet. 2011. PMID: 20825432

7

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.

8

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.

9

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.

10

Contribution of 3D ultrasound and fetal face studies to the prenatal diagnosis of Pallister-Killian syndrome.

Sananes N, Guigue V, Vayssiere C, Kohler M, Girard-Lemaire F, Flori E, Carelle-Calmels N, Boehm N, Samama B, Doray B, Favre R. Sananes N, et al. Among authors: doray b. J Matern Fetal Neonatal Med. 2010 Jun;23(6):558-62. doi: 10.3109/14767050903214558. J Matern Fetal Neonatal Med. 2010. PMID: 19718583 Free article.

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