Хайлтын үр дүнгүүд - Mugnier, C
- 3-н 1 - 3 үр дүнгүүдийг харуулж байна
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Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease -н Pelet, A, de Pontual, L, Clement-Ziza, M, Salomon, R, Mugnier, C, Matsuda, F, Lathrop, M, Munnich, A, Feingold, J, Lyonnet, S, Abel, L, Amiel, J
Хэвлэсэн 2005текст -
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Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency -н Lebon, S, Chol, M, Benit, P, Mugnier, C, Chretien, D, Giurgea, I, Kern, I, Girardin, E, Hertz-Pannier, L, de Lonlay, P, Rotig, A, Rustin, P, Munnich, A
Хэвлэсэн 2003текст