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Finocchiaro Gaetano
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http://hub.abes.fr/oup/periodical/humanmoleculargenetics/1995/volume_4/issue_1/101093hmg4119/authorship/6
http://hub.abes.fr/bmj/periodical/jnnp/2008/volume_79/issue_11/B35A82167B214C40E053120B220AF6DD/authorship/3
http://hub.abes.fr/springer/periodical/439/1995/volume_95/issue_6/B9280FB2F09B5EE6E053120B220A60AA/authorship/3
http://hub.abes.fr/springer/periodical/439/1994/volume_93/issue_3/B927DD9E86265D90E053120B220A1EA8/authorship/9
http://hub.abes.fr/springer/periodical/415/1984/volume_231/issue_1/B90B5E4613170505E053120B220A5FA7/authorship/2
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Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations
Electromyography and nerve conduction study in autosomal dominant olivopontocerebellar atrophy
Redefinition of the coding sequence of the MXI1 gene and identification of a polymorphic repeat in the 3′ non-coding region that allows the detection of loss of heterozygosity of chromosome 10q25 in glioblastomas
A multiple interval physical map of the pericentromeric region of human chromosome 10
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