Devillard F - Search Results

1

Microdeletion del(22)(q12.1) excluding the MN1 gene in a patient with craniofacial anomalies.

Bosson C, Devillard F, Satre V, Dieterich K, Ray PF, Morand B, Dubois-Teklali F, Vieville G, Andrieux J, Brouillet S, Amblard F, Jouk PS, Coutton C. Bosson C, et al. Among authors: devillard f. Am J Med Genet A. 2016 Feb;170A(2):498-503. doi: 10.1002/ajmg.a.37450. Epub 2015 Nov 6. Am J Med Genet A. 2016. PMID: 26545049

2

Population screening for aneuploidy using maternal age and ultrasound.

Cans C, Amblard F, Devillard F, Pison H, Jalbert P, Jouk PS. Cans C, et al. Among authors: devillard f. Prenat Diagn. 1998 Jul;18(7):683-92. Prenat Diagn. 1998. PMID: 9706649

3

Prenatal diagnosis of DMD in a female foetus affected by Turner syndrome.

Satre V, Monnier N, Devillard F, Amblard F, Lunardi J. Satre V, et al. Among authors: devillard f. Prenat Diagn. 2004 Nov;24(11):913-7. doi: 10.1002/pd.1031. Prenat Diagn. 2004. PMID: 15565644

4

Fine mapping of re-arranged Y chromosome in three infertile patients with non-obstructive azoospermia/cryptozoospermia.

Faure AK, Aknin-Seifer I, Satre V, Amblard F, Devillard F, Hennebicq S, Chouteau J, Bergues U, Levy R, Rousseaux S. Faure AK, et al. Among authors: devillard f. Hum Reprod. 2007 Jul;22(7):1854-60. doi: 10.1093/humrep/dem127. Hum Reprod. 2007. PMID: 17582144

5

Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism.

Devillard F, Guinchat V, Moreno-De-Luca D, Tabet AC, Gruchy N, Guillem P, Nguyen Morel MA, Leporrier N, Leboyer M, Jouk PS, Lespinasse J, Betancur C. Devillard F, et al. Am J Med Genet A. 2010 Sep;152A(9):2346-54. doi: 10.1002/ajmg.a.33601. Am J Med Genet A. 2010. PMID: 20684015 Free PMC article.

6

17p13.1 microduplication in a boy with Silver-Russell syndrome features and intellectual disability.

Coutton C, Devillard F, Vieville G, Amblard F, Lopez G, Jouk PS, Satre V. Coutton C, et al. Among authors: devillard f. Am J Med Genet A. 2012 Oct;158A(10):2564-70. doi: 10.1002/ajmg.a.35553. Epub 2012 Aug 17. Am J Med Genet A. 2012. PMID: 22903743

7

Interphase fluorescent in situ hybridization detection of the 7q11.23 chromosomal inversion in a clinical laboratory: automated versus manual scoring.

Nadeau G, Coutton C, Amblard F, Michalowicz G, Frasca S, Fertin A, Devillard F, Satre V, Usson Y, Jouk PS. Nadeau G, et al. Among authors: devillard f. Clin Chem Lab Med. 2013 Apr;51(4):e41-4. doi: 10.1515/cclm-2012-0416. Clin Chem Lab Med. 2013. PMID: 23072851 No abstract available.

8

190-kb duplication in 1p36.11 including PIGV and ARID1A genes in a girl with intellectual disability and hexadactyly.

Coutton C, Bidart M, Rendu J, Devillard F, Vieville G, Amblard F, Lopez G, Jouk PS, Satre V. Coutton C, et al. Among authors: devillard f. Clin Genet. 2013 Dec;84(6):596-9. doi: 10.1111/cge.12113. Epub 2013 Mar 25. Clin Genet. 2013. PMID: 23521658 No abstract available.

9

Currarino Syndrome and HPE Microform Associated with a 2.7-Mb Deletion in 7q36.3 Excluding SHH Gene.

Coutton C, Poreau B, Devillard F, Durand C, Odent S, Rozel C, Vieville G, Amblard F, Jouk PS, Satre V. Coutton C, et al. Among authors: devillard f. Mol Syndromol. 2014 Jan;5(1):25-31. doi: 10.1159/000355391. Epub 2013 Oct 2. Mol Syndromol. 2014. PMID: 24550762 Free PMC article.

10

Maternal complex chromosomal rearrangement leads to TCF12 microdeletion in a patient presenting with coronal craniosynostosis and intellectual disability.

Le Tanno P, Poreau B, Devillard F, Vieville G, Amblard F, Jouk PS, Satre V, Coutton C. Le Tanno P, et al. Among authors: devillard f. Am J Med Genet A. 2014 Jun;164A(6):1530-6. doi: 10.1002/ajmg.a.36467. Epub 2014 Mar 19. Am J Med Genet A. 2014. PMID: 24648389

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