TY - JFULL ID - 949872 TI - Genescreen : an international journal of medical genomics. PY - 2000 SN - 1466920X 14669218 PB - [Oxford, England] : Blackwell Science, DB - UniCat KW - Genetics KW - Genetics, Medical KW - Genetic Predisposition to Disease KW - Genetic Screening KW - Genome KW - Medical genetics KW - Genomics KW - Génétique médicale KW - Génomique KW - Periodicals. KW - Périodiques KW - Genomes KW - Human genome KW - Genetics, Medical. KW - Genome. KW - Genetic Testing. KW - Genetic Predisposition to Disease. KW - Genomes. KW - Human genome. KW - Medical genetics. KW - Chemistry KW - Health Sciences KW - Life Sciences KW - Biochemistry KW - Pathology KW - Predisposition, Genetic KW - Susceptibility, Genetic KW - Genetic Predisposition KW - Genetic Susceptibility KW - Genetic Predispositions KW - Genetic Susceptibilities KW - Predispositions, Genetic KW - Susceptibilities, Genetic KW - Disease Susceptibility KW - Predictive Genetic Testing KW - Predictive Testing, Genetic KW - Testing, Genetic Predisposition KW - Genetic Predisposition Testing KW - Genetic Predictive Testing KW - Genetic Screenings KW - Genetic Testing, Predictive KW - Predisposition Testing, Genetic KW - Screening, Genetic KW - Screenings, Genetic KW - Testing, Genetic KW - Testing, Genetic Predictive KW - Testing, Predictive Genetic KW - Human Genetics KW - Medical Genetics KW - Genetics, Human KW - genetics KW - diagnosis KW - Genetic Testing KW - Anticipation, Genetic KW - Genetic Association Studies KW - Gene-Environment Interaction KW - Prenatal Diagnosis KW - Preimplantation Diagnosis KW - Cytogenetic Analysis KW - Molecular Diagnostic Techniques KW - Databases, Genetic KW - Databases, Nucleic Acid KW - Genetic Privacy KW - Genes KW - Proteome KW - Anthropology, Physical KW - Chromosome Disorders KW - Sex Chromosome Disorders KW - Genetic Diseases, Inborn KW - Molecular Medicine KW - Human chromosomes KW - Haploidy KW - Clinical genetics KW - Diseases KW - Heredity of disease KW - Human genetics KW - Medical sciences KW - Genetic disorders KW - Genetic aspects UR - https://www.unicat.be/uniCat?func=search&query=sysid:949872 AB - ER -