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Deafness-family matters.
Roux AF. Roux AF. Eur J Hum Genet. 2022 Jan;30(1):5-6. doi: 10.1038/s41431-021-01006-5. Epub 2021 Nov 25. Eur J Hum Genet. 2022. PMID: 34819629 Free PMC article. No abstract available.
The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus.
Girardet A, Viart V, Plaza S, Daina G, De Rycke M, Des Georges M, Fiorentino F, Harton G, Ishmukhametova A, Navarro J, Raynal C, Renwick P, Saguet F, Schwarz M, SenGupta S, Tzetis M, Roux AF, Claustres M. Girardet A, et al. Among authors: roux af. Eur J Hum Genet. 2016 Apr;24(4):469-78. doi: 10.1038/ejhg.2015.99. Epub 2015 May 27. Eur J Hum Genet. 2016. PMID: 26014425 Free PMC article.
MobiDetails: online DNA variants interpretation.
Baux D, Van Goethem C, Ardouin O, Guignard T, Bergougnoux A, Koenig M, Roux AF. Baux D, et al. Among authors: roux af. Eur J Hum Genet. 2021 Feb;29(2):356-360. doi: 10.1038/s41431-020-00755-z. Epub 2020 Nov 7. Eur J Hum Genet. 2021. PMID: 33161418 Free PMC article.
Correction: MobiDetails: online DNA variants interpretation.
Baux D, Van Goethem C, Ardouin O, Guignard T, Bergougnoux A, Koenig M, Roux AF. Baux D, et al. Among authors: roux af. Eur J Hum Genet. 2021 Feb;29(2):361. doi: 10.1038/s41431-020-00789-3. Eur J Hum Genet. 2021. PMID: 33303978 Free PMC article. No abstract available.
Molecular epidemiology of DFNB1 deafness in France.
Roux AF, Pallares-Ruiz N, Vielle A, Faugère V, Templin C, Leprevost D, Artières F, Lina G, Molinari N, Blanchet P, Mondain M, Claustres M. Roux AF, et al. BMC Med Genet. 2004 Mar 6;5:5. doi: 10.1186/1471-2350-5-5. BMC Med Genet. 2004. PMID: 15070423 Free PMC article.
95 results