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Prenatal diagnosis of trisomy 9 mosaicism: two new cases.
Merino A, De Perdigo A, Nombalais F, Yvinec M, Le Roux MG, Bellec V. Merino A, et al. Among authors: le roux mg. Prenat Diagn. 1993 Oct;13(10):1001-7. doi: 10.1002/pd.1970131016. Prenat Diagn. 1993. PMID: 8309895
A new (old) deletion in the choroideremia gene.
Pascal O, Donnelly P, Fouanon C, Herbert O, Le Roux MG, Moisan JP. Pascal O, et al. Among authors: le roux mg. Hum Mol Genet. 1993 Sep;2(9):1489. doi: 10.1093/hmg/2.9.1489. Hum Mol Genet. 1993. PMID: 8242078 No abstract available.
Non-paternity and genetic counselling.
Le Roux MG, Pascal O, Andre MT, Herbert O, David A, Moisan JP. Le Roux MG, et al. Lancet. 1992 Sep 5;340(8819):607. doi: 10.1016/0140-6736(92)92139-7. Lancet. 1992. PMID: 1355175 No abstract available.
Missense mutation in the choroideremia gene.
Donnelly P, Menet H, Fouanon C, Herbert O, Moisan JP, Le Roux MG, Pascal O. Donnelly P, et al. Among authors: le roux mg. Hum Mol Genet. 1994 Jun;3(6):1017. doi: 10.1093/hmg/3.6.1017. Hum Mol Genet. 1994. PMID: 7951216 No abstract available.
VNTR at the DXYS14 locus.
Le Roux MG, Pascal O, Lostanlen A, Bérard I, Vergnaud O, Moisan JP. Le Roux MG, et al. Hum Mol Genet. 1994 Feb;3(2):389. doi: 10.1093/hmg/3.2.389-a. Hum Mol Genet. 1994. PMID: 8004126 No abstract available.
21 results