Odent S - Search Results

1

Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.

Jaillard S, Drunat S, Bendavid C, Aboura A, Etcheverry A, Journel H, Delahaye A, Pasquier L, Bonneau D, Toutain A, Burglen L, Guichet A, Pipiras E, Gilbert-Dussardier B, Benzacken B, Martin-Coignard D, Henry C, David A, Lucas J, Mosser J, David V, Odent S, Verloes A, Dubourg C. Jaillard S, et al. Among authors: odent s. Eur J Med Genet. 2010 Mar-Apr;53(2):66-75. doi: 10.1016/j.ejmg.2009.10.002. Epub 2009 Oct 28. Eur J Med Genet. 2010. PMID: 19878743 Free article.

2

[Argininosuccinic aciduria. A new case revealed by psychiatric disorders].

Odent S, Roussey M, Journel H, Betremieux P, David V, Le Marec B. Odent S, et al. J Genet Hum. 1989 Jan;37(1):39-42. J Genet Hum. 1989. PMID: 2715782 French.

3

[Reflections on 10 years of medically induced abortions in Ille-et-Vilaine].

Schneider S, Roussey M, Odent S, Debroise C, Poulain P, Jouan H, Milon J, Betremieux P, Journel H, Le Mee F, et al. Schneider S, et al. Among authors: odent s. J Gynecol Obstet Biol Reprod (Paris). 1994;23(2):157-65. J Gynecol Obstet Biol Reprod (Paris). 1994. PMID: 8040573 French.

4

Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20.

Dorval I, Odent S, Jezequel P, Journel H, Chauvel B, Dabadie A, Roussey M, Le Gall JY, Le Marec B, David V, et al. Dorval I, et al. Among authors: odent s. Hum Genet. 1993 Apr;91(3):254-6. doi: 10.1007/BF00218266. Hum Genet. 1993. PMID: 8097485

5

Opitz GBBB syndrome: chromosomal evidence of an X-linked form.

Verloes A, David A, Odent S, Toutain A, André MJ, Lucas J, Le Marec B. Verloes A, et al. Among authors: odent s. Am J Med Genet. 1995 Oct 23;59(1):123-8. doi: 10.1002/ajmg.1320590124. Am J Med Genet. 1995. PMID: 8849003

6

Central nervous system malformations and early end-stage renal disease in oro-facio-digital syndrome type I: a review.

Odent S, Le Marec B, Toutain A, David A, Vigneron J, Tréguier C, Jouan H, Milon J, Fryns JP, Verloes A. Odent S, et al. Am J Med Genet. 1998 Feb 3;75(4):389-94. Am J Med Genet. 1998. PMID: 9482645 Review.

7

Identification of novel L1CAM mutations using fluorescence-assisted mismatch analysis.

Saugier-Veber P, Martin C, Le Meur N, Lyonnet S, Munnich A, David A, Hénocq A, Héron D, Jonveaux P, Odent S, Manouvrier S, Moncla A, Morichon N, Philip N, Satge D, Tosi M, Frébourg T. Saugier-Veber P, et al. Among authors: odent s. Hum Mutat. 1998;12(4):259-66. doi: 10.1002/(SICI)1098-1004(1998)12:4<259::AID-HUMU7>3.0.CO;2-A. Hum Mutat. 1998. PMID: 9744477

8

FRAXE: the HindIII/OXE20 restriction polymorphism is not a rare variant.

Blayau M, Odent S, Dubourg C, David V. Blayau M, et al. Among authors: odent s. Hum Genet. 1998 Nov;103(5):626-7. doi: 10.1007/s004390050879. Hum Genet. 1998. PMID: 9860307 No abstract available.

9

Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. Online.

Dubourg C, Odent S, Fergelot P, Le Gall JY, David V, Blayau M. Dubourg C, et al. Among authors: odent s. Hum Mutat. 1999;13(2):173. doi: 10.1002/(SICI)1098-1004(1999)13:2<173::AID-HUMU20>3.0.CO;2-3. Hum Mutat. 1999. PMID: 10094565

10

Heterotaxy-neural tube defect and holoprosencephaly occuring independently in two sib fetuses.

Bonneau D, Maréchaud M, Odent S, Piegay I, Godard A, Amati P. Bonneau D, et al. Among authors: odent s. Am J Med Genet. 1999 Jun 4;84(4):373-6. doi: 10.1002/(sici)1096-8628(19990604)84:4<373::aid-ajmg13>3.0.co;2-8. Am J Med Genet. 1999. PMID: 10340655

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