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Ce livre fournit aux professionnels et aux étudiants les informations les plus récentes et les plus complètes sur la déficience intellectuelle et ses répercussions tant sur le plan neuropsychologique que psychopathologique. Il fait également le tour des prises en charge validées et adaptées selon l'étiologie de la déficience : autisme, trisomie 21 et autres anomalies chromosomiques, épilepsie, maladies infectieuses.
Déficience intellectuelle. --- Remédiation cognitive. --- Troubles de la cognition. --- Mental retardation --- Cognition disorders --- Intellectual disability. --- Troubles du développement --- Handicapés mentaux --- Troubles du comportement alimentaire --- Toxicomanie --- Troubles obsessionnels-compulsifs --- Neuropsychologie --- Déficience intellectuelle. --- Maladies chromosomiques. --- Neuropsychologie. --- Déficience intellectuelle --- Étiologie. --- Developmental disabilities --- Eating disorders --- Drug abuse --- Obsessive-compulsive disorder --- Neuropsychology --- Remédiation cognitive.
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Chromosome Aberrations. --- Chromosome Mapping. --- Cytogenetics. --- Karyotyping. --- Karyotype Analysis Methods --- Analysis Method, Karyotype --- Analysis Methods, Karyotype --- Karyotype Analysis Method --- Karyotypings --- Method, Karyotype Analysis --- Methods, Karyotype Analysis --- Chromosomes --- Cytogenetics --- Karyometry --- Karyotype --- Cytogenetic --- Cytogenetic Analysis --- Chromosome Disorders --- Sex Chromosome Disorders --- Genome Mapping --- Gene Mapping --- Linkage Mapping --- Chromosome Mappings --- Gene Mappings --- Genome Mappings --- Linkage Mappings --- Mapping, Chromosome --- Mapping, Gene --- Mapping, Genome --- Mapping, Linkage --- Mappings, Chromosome --- Mappings, Gene --- Mappings, Genome --- Mappings, Linkage --- Genetic Markers --- Gene Order --- Synteny --- Abnormalities, Autosome --- Abnormalities, Chromosomal --- Abnormalities, Chromosome --- Chromosomal Aberrations --- Chromosome Abnormalities --- Cytogenetic Abnormalities --- Autosome Abnormalities --- Cytogenetic Aberrations --- Aberration, Chromosomal --- Aberration, Chromosome --- Aberration, Cytogenetic --- Aberrations, Chromosomal --- Aberrations, Chromosome --- Aberrations, Cytogenetic --- Abnormalities, Cytogenetic --- Abnormality, Autosome --- Abnormality, Chromosomal --- Abnormality, Chromosome --- Abnormality, Cytogenetic --- Autosome Abnormality --- Chromosomal Aberration --- Chromosomal Abnormalities --- Chromosomal Abnormality --- Chromosome Aberration --- Chromosome Abnormality --- Cytogenetic Aberration --- Cytogenetic Abnormality --- Genetics, Medical --- abnormalities --- CHROMOSOME ABERRATIONS --- CHROMOSOME ABNORMALITIES --- CHROMOSOME MAPPING --- CYTOGENETICS --- Karyotyping --- atlases --- atlases. --- Chromosome aberrations --- Chromosome abnormalities --- Chromosome mapping --- Atlases. --- Chromosome Aberrations --- Chromosome Mapping --- Maladies chromosomiques. --- Genetic Diseases, Inborn --- Genes --- Maps --- Nomenclature. --- Maps. --- Genetic Diseases, Inborn.
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A popular and easy-to-use guide, this book is a must-have tool for clinical consultations in genetics and genomic medicine. Ideal for quick reference during practice, it covers the process of diagnosis, investigation, management, and counselling for patients. With a strong evidence base and international guidelines, it puts reliable and trustworthy guidance at your fingertips. Designed for use as a first-line guide, the A to Z format ensures it's accessible, and the simple layout makes it easy to assimilate information. Highly illustrated, the book also contains up-to-date glossaries of terms used in genetics and dysmorphology providing quick reference for key concepts. The second edition is an eagerly anticipated update of the gold standard in the specialty. It covers new developments in the field, particularly the advent of genome-wide sequencing and major updates in cancer. Fifteen new topics have been added, including Sudden cardiac death, Neonatal screening, and Ciliopathies. The authors have used their experience to devise a practical clinical approach to many common genetic referrals, both outpatient and ward based. The most common Mendelian disorders, chromosomal disorders, congenital anomalies and syndromes are all covered, and where available diagnostic criteria are included. In addition there are chapters on familial cancer and pregnancy-related topics such as fetal anomalies, teratogens, prenatal and pre-implantation diagnosis and non-invasive prenatal testing. The book also provides information on the less common situations where management is particularly complex. Both practical and pertinent, Oxford Desk Reference: Clinical Genetics and Genomics is the companion you need by your side during clinical consultations.
Genetics, Medical --- Genomics --- Chromosome Aberrations --- Genetic Diseases, Inborn --- Genetic Predisposition to Disease --- Medical genetics. --- Genomics. --- Génétique médicale --- Chromosomes humains --- Aberration chromosomique --- Maladies héréditaires --- Prédisposition (médecine) --- Anomalies --- Maladies chromosomiques. --- Aberrations chromosomiques. --- Genetics, Medical. --- Chromosome Aberrations. --- Genetic Diseases, Inborn. --- Genetic Predisposition to Disease. --- Genetic Diseases --- Genetic Disorders --- Hereditary Disease --- Inborn Genetic Diseases --- Single-Gene Defects --- Hereditary Diseases --- Defect, Single-Gene --- Defects, Single-Gene --- Disease, Genetic --- Disease, Hereditary --- Disease, Inborn Genetic --- Diseases, Genetic --- Diseases, Hereditary --- Diseases, Inborn Genetic --- Disorder, Genetic --- Disorders, Genetic --- Genetic Disease --- Genetic Disease, Inborn --- Genetic Disorder --- Inborn Genetic Disease --- Single Gene Defects --- Single-Gene Defect --- Comparative Genomics --- Comparative Genomic --- Genomic, Comparative --- Genomics, Comparative --- Human Genome Project --- Genome --- Predisposition, Genetic --- Susceptibility, Genetic --- Genetic Predisposition --- Genetic Susceptibility --- Genetic Predispositions --- Genetic Susceptibilities --- Predispositions, Genetic --- Susceptibilities, Genetic --- Disease Susceptibility --- Genetic Testing --- Anticipation, Genetic --- Genetic Association Studies --- Gene-Environment Interaction --- Abnormalities, Autosome --- Abnormalities, Chromosomal --- Abnormalities, Chromosome --- Chromosomal Aberrations --- Chromosome Abnormalities --- Cytogenetic Abnormalities --- Autosome Abnormalities --- Cytogenetic Aberrations --- Aberration, Chromosomal --- Aberration, Chromosome --- Aberration, Cytogenetic --- Aberrations, Chromosomal --- Aberrations, Chromosome --- Aberrations, Cytogenetic --- Abnormalities, Cytogenetic --- Abnormality, Autosome --- Abnormality, Chromosomal --- Abnormality, Chromosome --- Abnormality, Cytogenetic --- Autosome Abnormality --- Chromosomal Aberration --- Chromosomal Abnormalities --- Chromosomal Abnormality --- Chromosome Aberration --- Chromosome Abnormality --- Cytogenetic Aberration --- Cytogenetic Abnormality --- Chromosomes --- Cytogenetics --- Cytogenetic Analysis --- Medical Genetics --- Anthropology, Physical --- Chromosome Disorders --- Sex Chromosome Disorders --- Molecular Medicine --- genetics --- abnormalities --- Génétique médicale --- Maladies héréditaires --- Prédisposition (médecine)
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