TY - JFULL ID - 4889056 TI - Human genome variation. PY - 2014 SN - 2054345X PB - [London] : Nature Publishing Group, DB - UniCat KW - Genetics, Medical. KW - Genetic Diseases, Inborn. KW - Medical genetics KW - Génétique médicale KW - Periodicals. KW - Périodiques KW - Medical genetics. KW - Clinical genetics KW - Diseases KW - Heredity of disease KW - Genetic Diseases KW - Genetic Disorders KW - Hereditary Disease KW - Inborn Genetic Diseases KW - Single-Gene Defects KW - Hereditary Diseases KW - Defect, Single-Gene KW - Defects, Single-Gene KW - Disease, Genetic KW - Disease, Hereditary KW - Disease, Inborn Genetic KW - Diseases, Genetic KW - Diseases, Hereditary KW - Diseases, Inborn Genetic KW - Disorder, Genetic KW - Disorders, Genetic KW - Genetic Disease KW - Genetic Disease, Inborn KW - Genetic Disorder KW - Inborn Genetic Disease KW - Single Gene Defects KW - Single-Gene Defect KW - Human Genetics KW - Medical Genetics KW - Genetics, Human KW - Genetic aspects KW - GenomeVariation KW - Gene Mutation KW - Rare diseases KW - disease-associated genes KW - Human genetics KW - Medical sciences KW - Pathology KW - Genetic disorders KW - Genetics, Medical KW - Anthropology, Physical KW - Chromosome Disorders KW - Sex Chromosome Disorders KW - Genetic Diseases, Inborn KW - Molecular Medicine KW - genomevariation KW - gene mutation KW - rare diseases KW - Evolution. Phylogeny KW - Genetics KW - Genoma humà. KW - Revistes electròniques. KW - Revistes digitals KW - Revistes en línia KW - Revistes on line KW - Revistes per Internet KW - Publicacions electròniques KW - Revistes KW - Genomes KW - Cromosomes humans KW - Genètica humana UR - https://www.unicat.be/uniCat?func=search&query=sysid:4889056 AB - ER -