Girard-Lemaire F - 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. 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

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: girard lemaire f. Eur J Hum Genet. 2005 Sep;13(9):1013-8. doi: 10.1038/sj.ejhg.5201442. Eur J Hum Genet. 2005. PMID: 15915162

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: girard lemaire f. Eur J Hum Genet. 2004 Mar;12(3):181-6. doi: 10.1038/sj.ejhg.5201134. Eur J Hum Genet. 2004. PMID: 14694357

5

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. Prenat Diagn. 2002 Dec;22(13):1177-80. doi: 10.1002/pd.473. Prenat Diagn. 2002. PMID: 12478628 Review.

6

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.

7

Phenotype in X chromosome rearrangements: pitfalls of X inactivation study.

Schluth C, Cossée M, Girard-Lemaire F, Carelle N, Dollfus H, Jeandidier E, Flori E. Schluth C, et al. Among authors: girard lemaire f. Pathol Biol (Paris). 2007 Feb;55(1):29-36. doi: 10.1016/j.patbio.2006.04.003. Epub 2006 May 11. Pathol Biol (Paris). 2007. PMID: 16690229

8

Genetic mosaicism in an acquired inflammatory dermatosis following the lines of Blaschko.

Lipsker D, Cribier B, Girard-Lemaire F, Flori E, Grosshans E. Lipsker D, et al. Arch Dermatol. 2000 Jun;136(6):805-7. doi: 10.1001/archderm.136.6.805. Arch Dermatol. 2000. PMID: 10871961 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: girard lemaire f. 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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

18 results

Search Page

Filters