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F Cailloux

Showing results (1-10 of 3) with videos related to

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Human Genetics|August 1, 1995
Dinucleotide repeat polymorphism in the proteolipoprotein (PLP) geneC Mimault, F Cailloux, G Giraud, et al.
American Journal of Human Genetics|July 27, 1999
Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher Disease: duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not. The Clinical European Network on Brain Dysmyelinating DiseaseC Mimault, G Giraud, V Courtois, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating DiseaseF Cailloux, F Gauthier-Barichard, C Mimault, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Human Genetics|August 1, 1995
Dinucleotide repeat polymorphism in the proteolipoprotein (PLP) geneC Mimault, F Cailloux, G Giraud, et al.
American Journal of Human Genetics|July 27, 1999
Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher Disease: duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not. The Clinical European Network on Brain Dysmyelinating DiseaseC Mimault, G Giraud, V Courtois, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating DiseaseF Cailloux, F Gauthier-Barichard, C Mimault, et al.
Pageof 1