Labrune P - Search Results

1

Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndrome.

Petit FM, Gajdos V, Parisot F, Capel L, Aboura A, Lachaux A, Tachdjian G, Poüs C, Labrune P. Petit FM, et al. Among authors: labrune p. Eur J Hum Genet. 2005 Mar;13(3):278-82. doi: 10.1038/sj.ejhg.5201342. Eur J Hum Genet. 2005. PMID: 15586176

2

Prenatal diagnosis of Crigler-Najjar syndrome type I by single-strand conformation polymorphism (SSCP).

Francoual J, Trioche P, Mokrani C, Seboui H, Khrouf N, Chalas J, Clement M, Capel L, Tachdjian G, Labrune P. Francoual J, et al. Among authors: labrune p. Prenat Diagn. 2002 Oct;22(10):914-6. doi: 10.1002/pd.443. Prenat Diagn. 2002. PMID: 12378576

3

The Tunisian population history through the Crigler-Najjar type I syndrome.

Petit FM, Bézieau S, Gajdos V, Parisot F, Scoul C, Capel L, Stozinic V, Khrouf N, M'Rad R, Koshy A, Mollet-Boudjemline A, Francoual J, Labrune P. Petit FM, et al. Among authors: labrune p. Eur J Hum Genet. 2008 Jul;16(7):848-53. doi: 10.1038/sj.ejhg.5201989. Epub 2008 Jan 16. Eur J Hum Genet. 2008. PMID: 18197191

4

A new mutation in the AFP gene responsible for a total absence of alpha feto-protein on second trimester maternal serum screening for Down syndrome.

Petit FM, Hébert M, Picone O, Brisset S, Maurin ML, Parisot F, Capel L, Benattar C, Sénat MV, Tachdjian G, Labrune P. Petit FM, et al. Among authors: labrune p. Eur J Hum Genet. 2009 Mar;17(3):387-90. doi: 10.1038/ejhg.2008.186. Epub 2008 Oct 15. Eur J Hum Genet. 2009. PMID: 18854864 Free PMC article.

5

Recurrent 70.8 Mb 4q22.2q32.3 duplication due to ovarian germinal mosaicism.

Tosca L, Brisset S, Petit FM, Lecerf L, Rousseau G, Bas C, Laroudie M, Maurin ML, Tapia S, Picone O, Prevot S, Goossens M, Labrune P, Tachdjian G. Tosca L, et al. Among authors: labrune p. Eur J Hum Genet. 2010 Aug;18(8):882-8. doi: 10.1038/ejhg.2010.46. Epub 2010 Apr 28. Eur J Hum Genet. 2010. PMID: 20424646 Free PMC article.

6

Early and rapid prenatal diagnosis of monosomy 2q36.1 in trophoblast cells.

Tachdjian G, Aboura A, Brisset S, Dommergues M, Gajdos V, Labrune P. Tachdjian G, et al. Among authors: labrune p. Fetal Diagn Ther. 2006;21(5):428-32. doi: 10.1159/000093885. Fetal Diagn Ther. 2006. PMID: 16912492

7

Successful pregnancy in a Crigler-Najjar type I patient treated by phototherapy and semimonthly albumin infusions.

Gajdos V, Petit F, Trioche P, Mollet-Boudjemline A, Chauveaud A, Myara A, Trivin F, Francoual J, Labrune P. Gajdos V, et al. Among authors: labrune p. Gastroenterology. 2006 Sep;131(3):921-4. doi: 10.1053/j.gastro.2006.07.005. Gastroenterology. 2006. PMID: 16952560 No abstract available.

8

Large deletion in UGT1A1 gene encompassing the promoter and the exon 1 responsible for Crigler-Najjar type I syndrome.

Petit FM, Hébert M, Gajdos V, Capel L, M'Rad R, Labrune P. Petit FM, et al. Among authors: labrune p. Haematologica. 2008 Oct;93(10):1590-1. doi: 10.3324/haematol.13295. Epub 2008 Aug 12. Haematologica. 2008. PMID: 18698077 Free article. No abstract available.

9

Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15.

L'Herminé AC, Aboura A, Brisset S, Cuisset L, Castaigne V, Labrune P, Frydman R, Tachdjian G. L'Herminé AC, et al. Among authors: labrune p. Prenat Diagn. 2003 Nov;23(11):938-43. doi: 10.1002/pd.732. Prenat Diagn. 2003. PMID: 14634983

10

Allelic heterogeneity of Crigler-Najjar type I syndrome: a study of 24 cases.

Petit FM, Gajdos V, Francoual J, Capel L, Parisot F, Poüs C, Labrune P. Petit FM, et al. Among authors: labrune p. Clin Genet. 2004 Dec;66(6):571-2. doi: 10.1111/j.1399-0004.2004.00371.x. Clin Genet. 2004. PMID: 15521991 No abstract available.

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