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المؤلفون: Hilda Bibas Bonet, Lucía Paola Rey, Maria Luisa Mostacciuolo, Larissa Arning, Anna Mazzeo, Judith Koetting, Mirta Esther Abdala, Wanda M. Gerding, Roque Carrero-Valenzuela
المصدر: Molecular and cellular probes. 27(3-4)
مصطلحات موضوعية: Male, Argentina, Biology, Polymorphism, Single Nucleotide, DNA sequencing, Connexins, Cx32, Exon, Hereditary motor sensory peripheral neuropathy, Charcot-Marie-Tooth Disease, CMT X1, medicine, Humans, HMSN, Polymorphism, Allele, education, Molecular Biology, Gene, Alleles, Genetics, education.field_of_study, Haplotype, GJB1, Single Nucleotide, Cell Biology, medicine.disease, Molecular biology, Pedigree, genomic DNA, Phenotype, Haplotypes, Mutation, Connexin 32, Female, Microsatellite Repeats, Hereditary motor and sensory neuropathy
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2دورية أكاديمية
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