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SMN gene analysis of the spinal form of Charcot-Marie-Tooth disease.
Hanash A, Leguern E, Birouk N, Clermont O, Pouget J, Bouche P, Munnich A, Brice A, Melki J. Hanash A, et al. Among authors: clermont o. J Med Genet. 1997 Jun;34(6):507-8. doi: 10.1136/jmg.34.6.507. J Med Genet. 1997. PMID: 9192274 Free PMC article.
Trinucleotide repeat polymorphism at the D5S556 locus.
Burlet P, Abdelhak S, Pascal F, Clermont O, Paul B, Munnich A, Melki J. Burlet P, et al. Among authors: clermont o. Hum Mol Genet. 1993 Aug;2(8):1328. doi: 10.1093/hmg/2.8.1328. Hum Mol Genet. 1993. PMID: 8401523 No abstract available.
SMN gene deletions in adult-onset spinal muscular atrophy.
Clermont O, Burlet P, Lefebvre S, Bürglen L, Munnich A, Melki J. Clermont O, et al. Lancet. 1995 Dec 23-30;346(8991-8992):1712-3. doi: 10.1016/s0140-6736(95)92881-2. Lancet. 1995. PMID: 8551862 No abstract available.
147 results