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المؤلفون: Constantin Lupu, Janina Hantke, Ivailo Tournev, Tamara Rogers, Velina Guergueltcheva, Jaume Colomer, Jon Andoni Urtizberea, Axinia Corches, Luba Kalaydjieva, Lisa French, Luciano Merlini, P. K. Thomas
المصدر: Neuromuscular disorders : NMD. 13(9)
مصطلحات موضوعية: Male, Candidate gene, Genetic Linkage, Biology, Bac clone, Charcot-Marie-Tooth Disease, Databases, Genetic, medicine, Humans, Gene, Genotyping, Genetics (clinical), Sequence (medicine), Genetics, Polymorphism, Genetic, Chromosomes, Human, Pair 10, Chromosome Mapping, medicine.disease, Pedigree, Europe, Phenotype, Neurology, Genetic marker, Pediatrics, Perinatology and Child Health, Mutation (genetic algorithm), Female, Neurology (clinical), Hereditary motor and sensory neuropathy, Hereditary Sensory and Motor Neuropathy
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::932c47d3fee0300e48bd16843d526320Test
https://pubmed.ncbi.nlm.nih.gov/14561496Test -
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المؤلفون: Jaume Colomer, Yesim Parman, Rebecca Gooding, Dora Angelicheva, R. H. M. King, Jaume Bertranpetit, Luba Kalaydjieva, David Chandler, L. Marns
المصدر: Scopus-Elsevier
مصطلحات موضوعية: Male, Neuromuscular disease, Genetic Linkage, Molecular Sequence Data, Population, Biology, Arginine, Electronic Letter, Genetic linkage, SH3TC2, Genetics, medicine, Humans, Child, education, Genetics (clinical), Family Health, education.field_of_study, Base Sequence, Models, Genetic, Haplotype, Intracellular Signaling Peptides and Proteins, Peripheral Nervous System Diseases, Proteins, medicine.disease, Founder Effect, Pedigree, Phenotype, Peripheral neuropathy, Spain, Mutation, Mutation (genetic algorithm), Female, Founder effect
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2b054dc2c1001b826acfb1650295f9eTest
https://doi.org/10.1136/jmg.2005.034132Test