Girardet A - Search Results

1

New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?

Barat-Houari M, Nguyen K, Bernard R, Fernandez C, Vovan C, Bareil C, Khau Van Kien P, Thorel D, Tuffery-Giraud S, Vasseur F, Attarian S, Pouget J, Girardet A, Lévy N, Claustres M. Barat-Houari M, et al. Among authors: girardet a. Eur J Hum Genet. 2010 May;18(5):533-8. doi: 10.1038/ejhg.2009.207. Epub 2009 Nov 25. Eur J Hum Genet. 2010. PMID: 19935833 Free PMC article.

2

Amplification of the RB1.20 polymorphism in single spermatozoa.

Girardet A, Pellestor F, Tuffery S, Claustres M, Munier F, Duperray C. Girardet A, et al. J Assist Reprod Genet. 1997 Mar;14(3):177-9. doi: 10.1007/BF02766137. J Assist Reprod Genet. 1997. PMID: 9090563 Free PMC article. No abstract available.

3

[Retinoblastoma: importance of genetic counseling].

Girardet A, Beaufrere L, Tuffery S, Claustres M, Pellestor F. Girardet A, et al. J Fr Ophtalmol. 1998 Apr;21(4):295-301. J Fr Ophtalmol. 1998. PMID: 9759420 Review. French. No abstract available.

4

[Update on a diagnostic test for choroideremia: the protein truncation test (PTT)].

Beaufrere L, Girardet A, Arnaud B, Claustres M, Tuffery S. Beaufrere L, et al. Among authors: girardet a. J Fr Ophtalmol. 1998 May;21(5):345-50. J Fr Ophtalmol. 1998. PMID: 9759428 French.

5

Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African family.

Macari F, Lautier C, Girardet A, Dadoun F, Darmon P, Dutour A, Renard E, Bouvagnet P, Claustres M, Oliver C, Grigorescu F. Macari F, et al. Among authors: girardet a. Hum Genet. 1998 Dec;103(6):658-61. doi: 10.1007/s004390050887. Hum Genet. 1998. PMID: 9921899

6

Direct estimation of the recombination frequency between the RB1 gene and two closely linked microsatellites using sperm typing.

Girardet A, Lien S, Leeflang EP, Beaufrère L, Tuffery S, Munier F, Arnheim N, Claustres M, Pellestor F. Girardet A, et al. Eur J Hum Genet. 1999 Feb-Mar;7(2):239-42. doi: 10.1038/sj.ejhg.5200250. Eur J Hum Genet. 1999. PMID: 10196709

7

Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typing.

Girardet A, McPeek MS, Leeflang EP, Munier F, Arnheim N, Claustres M, Pellestor F. Girardet A, et al. Am J Hum Genet. 2000 Jan;66(1):167-75. doi: 10.1086/302715. Am J Hum Genet. 2000. PMID: 10631148 Free PMC article.

8

First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markers.

Girardet A, Hamamah S, Anahory T, Déchaud H, Sarda P, Hédon B, Demaille J, Claustres M. Girardet A, et al. Mol Hum Reprod. 2003 Feb;9(2):111-6. doi: 10.1093/molehr/gag014. Mol Hum Reprod. 2003. PMID: 12569181

9

Rapid detection of the deltaF508 mutation in single cells using DHPLC: implications for preimplantation genetic diagnosis.

Girardet A, Cathala P, Claustres M. Girardet A, et al. J Assist Reprod Genet. 2003 Apr;20(4):153-6. doi: 10.1023/a:1022981103862. J Assist Reprod Genet. 2003. PMID: 12762414 Free PMC article.

10

Specific detection of deleted and non-deleted dystrophin exons together with gender assignment in preimplantation genetic diagnosis of Duchenne muscular dystrophy.

Girardet A, Hamamah S, Déchaud H, Anahory T, Coubes C, Hédon B, Demaille J, Claustres M. Girardet A, et al. Mol Hum Reprod. 2003 Jul;9(7):421-7. doi: 10.1093/molehr/gag050. Mol Hum Reprod. 2003. PMID: 12802049

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