Search Results - "Bachelot, M. F"

Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q by Melki, J, Abdelhak, S, Sheth, Peter, Bachelot, M. F, Burlet, Peter, Marcadet, Alun, Aicardi, J, Barois, Alun, Carriere, J. P, Fardeau, M, Fontan, D, Ponsot, G, Billette, T, Angelini, C, Barbosa, C, Ferriere, G, Lanzi, G, Ottolini, Alun, Babron, M. C, Cohen, D, Hanauer, Alun, Clerget-Darpoux, F, Lathrop, M, Munnich, Alun, Frezal, J

“…Proximal spinal muscular atrophies represent the second most common fatal, autosomal recessive disorder after cystic fibrosis. The childhood form is…”
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In situ hybridization of two markers closely flanking the spinal muscular atrophy gene to 5q12----q13.3 by Mattei, M G, Melki, J, Bachelot, M F, Abdelhak, S, Burlet, P, Frézal, J, Munnich, A

“…In order to refine the physical location of the p105-153Ra and M4 probes which closely flank the spinal muscular atrophy gene (SMA) on human chromosome 5q, in…”
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Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5 by SHETH, P, ABDELHAK, S, MELKI, J, BACHELOT, ML. F, BURLET, P, MASSET, M, HILLAIRE, D, CLERGET-DARPOUX, F, FREZAL, J, LATHROP, G. M, MUNNICH, A

“…The proximal spinal muscular atrophies (SMA) represent the second most common autosomal recessive disorder, after cystic fibrosis. The gene responsible for…”
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A PstI polymorphism at the D5S39 locus by Abdelhak, S, Melki, J, Bachelot, M F, Burlet, P, Sheth, P, Frézal, J, Munnich, A

“…Images…”
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Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy Investigators by Melki, J, Sheth, P, Abdelhak, S, Burlet, P, Bachelot, M F, Lathrop, M G, Frezal, J, Munnich, A

“…Linkage analysis in twenty-five families with acute (type I) spinal muscular atrophy (SMA) showed that the mutant gene responsible for the disorder is tightly…”
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