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"Since its introduction in 2012, cell-free (cf) DNA based Non-Invasive Prenatal Testing (NIPT) has been employed to test for fetal chromosome abnormalities, and gene mutations that lead to a variety of genetic conditions, by millions of pregnant women, in more than 90 countries worldwide. With Noninvasive Prenatal Testing (NIPT): Applied Genomics in Prenatal Screening and Diagnosis, Dr Lieve Page-Christiaens and Dr Hanns-Georg Klein have compiled the first authoritative volume on cfDNA NIPT methods and their clinical implementation"--Publisher's description.
Genetics --- Prenatal diagnosis. --- Diagnosis, Noninvasive. --- Genetic Testing. --- Prenatal Diagnosis. --- DNA --- blood.
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Cattle --- Fertility --- Mutation. --- Genetic Testing --- Bovins --- Fécondité --- Mutation (biologie) --- Dépistage génétique --- genetics. --- embryology. --- methods. --- Génétique. --- Embryologie. --- Chez les animaux. --- Méthodologie. --- Mutation --- genetics
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"Since its introduction in 2012, cell-free (cf) DNA based Non-Invasive Prenatal Testing (NIPT) has been employed to test for fetal chromosome abnormalities, and gene mutations that lead to a variety of genetic conditions, by millions of pregnant women, in more than 90 countries worldwide. With Noninvasive Prenatal Testing (NIPT): Applied Genomics in Prenatal Screening and Diagnosis, Dr Lieve Page-Christiaens and Dr Hanns-Georg Klein have compiled the first authoritative volume on cfDNA NIPT methods and their clinical implementation"--Publisher's description.
Prenatal diagnosis. --- Diagnosis, Noninvasive. --- Genetic Testing. --- Prenatal Diagnosis. --- DNA --- blood. --- Antenatal Diagnosis --- Antenatal Screening --- Diagnosis, Antenatal --- Diagnosis, Intrauterine --- Prenatal Screening --- Diagnosis, Prenatal --- Intrauterine Diagnosis --- Antenatal Diagnoses --- Antenatal Screenings --- Diagnoses, Antenatal --- Diagnoses, Intrauterine --- Diagnoses, Prenatal --- Intrauterine Diagnoses --- Prenatal Diagnoses --- Prenatal Screenings --- Screening, Antenatal --- Screening, Prenatal --- Screenings, Antenatal --- Screenings, Prenatal --- Genetic Testing --- Neonatal Screening --- Preimplantation Diagnosis --- Genetic Services --- Genetic Screening --- Predictive Genetic Testing --- Predictive Testing, Genetic --- Testing, Genetic Predisposition --- Genetic Predisposition Testing --- Genetic Predictive Testing --- Genetic Screenings --- Genetic Testing, Predictive --- Predisposition Testing, Genetic --- Screening, Genetic --- Screenings, Genetic --- Testing, Genetic --- Testing, Genetic Predictive --- Testing, Predictive Genetic --- Genetic Predisposition to Disease --- Prenatal Diagnosis --- Cytogenetic Analysis --- Molecular Diagnostic Techniques --- Databases, Genetic --- Databases, Nucleic Acid --- Genetic Privacy --- Diagnostic tests, Noninvasive --- Noninvasive diagnosis --- Noninvasive diagnostic tests --- Function tests (Medicine) --- Antenatal diagnosis --- Intrauterine diagnosis --- Prenatal testing --- Diagnosis --- Obstetrics --- diagnosis --- Fetal Diagnosis --- Fetal Imaging --- Fetal Screening --- Diagnosis, Fetal --- Fetal Diagnoses --- Fetal Imagings --- Fetal Screenings --- Imaging, Fetal --- Screening, Fetal
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Richly illustrated and comprehensive in scope, Obstetric Imaging, 2nd Edition, provides up-to-date, authoritative guidelines for more than 200 obstetric conditions and procedures, keeping you at the forefront of this fast-changing field. This highly regarded reference covers the extensive and ongoing advances in maternal and fetal imaging in a concise, newly streamlined format for quicker access to common and uncommon findings. Detailed, expert guidance, accompanied by superb, high-quality images, helps you make the most of new technologies and advances in obstetric imaging. -- Publisher
Congenital Abnormalities --- Fetus --- Prenatal Diagnosis. --- diagnostic imaging. --- abnormalities. --- Antenatal Diagnosis --- Antenatal Screening --- Diagnosis, Antenatal --- Diagnosis, Intrauterine --- Prenatal Screening --- Diagnosis, Prenatal --- Fetal Diagnosis --- Fetal Imaging --- Fetal Screening --- Intrauterine Diagnosis --- Antenatal Diagnoses --- Antenatal Screenings --- Diagnosis, Fetal --- Fetal Diagnoses --- Fetal Imagings --- Fetal Screenings --- Imaging, Fetal --- Intrauterine Diagnoses --- Prenatal Diagnoses --- Prenatal Screenings --- Screening, Antenatal --- Screening, Fetal --- Screening, Prenatal --- Genetic Testing --- Neonatal Screening --- Preimplantation Diagnosis --- Genetic Services
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"Advances in several different areas of the biosciences are coming together in ways that will change human reproduction forever. Vast improvements in the speed, accuracy, and cost of sequencing the entire human genome greatly increases the genetic information prospective parents can learn about their possible children. Rapid progress in stem cell research makes it likely that in twenty years or so, we will be able to make eggs and sperm from the skin cells of people--mature people, old people, children, and even from cells from the dead or the never born. Combining the eggs and sperm will make embryos in a potentially limitless supply; using a technique called preimplantation genetic diagnosis (PGD), which has been in limited but safe use in people for over twenty-five years, a few cells can be plucked from those embryos and have their genomes entirely sequenced. The result, which the author calls "Easy PGD," will give parents (or others) unprecedented power to select embryos for transfer into wombs and eventual birth as babies, based their predictable genetic traits. Those traits will include early-onset and terrible diseases; other, later or lesser, disease risks; cosmetic traits, some behavioral traits; and, last but not least "boy or girl." This book describes the background science of Easy PGD, lays out its pathway to widespread acceptance and use, and explores some of the many ethical, legal, and social issues it will raise. One thing seems very clear: after Easy PGD, making babies will change forever--and so will humanity."--
Preimplantation genetic diagnosis. --- Preimplantation genetic diagnosis --- Human reproduction. --- Preimplantation Diagnosis --- Reproductive Medicine --- Genetic Testing --- Reproduction --- 618.3 --- Human Reproductive Index --- Human Reproductive Indexes --- Reproductive Period --- Human Reproductive Indices --- Index, Human Reproductive --- Indexes, Human Reproductive --- Indices, Human Reproductive --- Period, Reproductive --- Periods, Reproductive --- Reproductive Index, Human --- Reproductive Indices, Human --- Reproductive Periods --- Genetic Screening --- Predictive Genetic Testing --- Predictive Testing, Genetic --- Testing, Genetic Predisposition --- Genetic Predisposition Testing --- Genetic Predictive Testing --- Genetic Screenings --- Genetic Testing, Predictive --- Predisposition Testing, Genetic --- Screening, Genetic --- Screenings, Genetic --- Testing, Genetic --- Testing, Genetic Predictive --- Testing, Predictive Genetic --- Genetic Predisposition to Disease --- Prenatal Diagnosis --- Cytogenetic Analysis --- Molecular Diagnostic Techniques --- Databases, Genetic --- Databases, Nucleic Acid --- Genetic Privacy --- Human physiology --- Reproductive health --- Reproductive rights --- Preembryo diagnosis --- Preimplantation diagnosis --- Prenatal diagnosis --- Moral and ethical aspects. --- ethics --- trends --- pathologie van de zwangerschap --- diagnosis --- Human reproduction --- Moral and ethical aspects --- Human reproductive technology --- Genetic engineering. --- Beroepsethiek. Deontologie --- Medisch recht --- Menselijke genetica --- Diagnostic préimplantatoire. --- Diagnostic préimplantatoire --- Reproduction humaine --- Aspect moral. --- Reproductive technology --- Techniques artificielles de la reproduction --- Law and legislation --- Droit --- Professional ethics. Deontology --- Medical law --- Human genetics --- Preimplantation genetic diagnosis - Moral and ethical aspects
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The Tietz Textbook of Clinical Chemistry and Molecular Diagnostics, 6th Edition provides the most current and authoritative guidance on selecting, performing, and evaluating the results of new and established laboratory tests. This classic clinical chemistry reference offers encyclopedic coverage detailing everything you need to know, including: analytical criteria for the medical usefulness of laboratory tests, variables that affect tests and results, laboratory medicine, applications of statistical methods, and most importantly clinical utility and interpretation of laboratory tests. It is THE definitive reference in clinical chemistry and molecular diagnostics, now fully searchable and with quarterly content updates, podcasts, clinical cases, animations, and extended content online through Expert Consult.
Clinical Chemistry Tests. --- Chemistry, Clinical --- Molecular Diagnostic Techniques. --- Molecular Diagnostic Technics --- Molecular Diagnostic Testing --- Diagnostic Technic, Molecular --- Diagnostic Technics, Molecular --- Diagnostic Technique, Molecular --- Diagnostic Techniques, Molecular --- Diagnostic Testing, Molecular --- Molecular Diagnostic Technic --- Molecular Diagnostic Technique --- Technic, Molecular Diagnostic --- Technics, Molecular Diagnostic --- Technique, Molecular Diagnostic --- Techniques, Molecular Diagnostic --- Testing, Molecular Diagnostic --- Genetic Testing --- Cytogenetic Analysis --- Chemistry Test, Clinical --- Clinical Chemistry Test --- Test, Clinical Chemistry --- Tests, Clinical Chemistry --- Chemistry Tests, Clinical --- methods. --- Clinical chemistry --- Molecular diagnosis --- Methods --- Clinical Chemistry Tests --- Molecular Diagnostic Techniques --- Diagnostic biochemistry --- Diagnostic chemistry --- Medical chemistry --- methods --- Human biochemistry --- Semiology. Diagnosis. Symptomatology --- Biochemistry --- Diagnosis, Laboratory --- moleculaire biologie --- klinische chemie --- Molecular Testing --- Testing, Molecular --- Pathological biochemistry
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"The Handbook provides an essential resource at the interface of Genomics, Health and Society, and forms a crucial research tool for both new students and established scholars across biomedicine and social sciences. Building from and extending the first Routledge Handbook of Genetics and Society, the book offers a comprehensive introduction to pivotal themes within the field, an overview of the current state of the art knowledge on genomics, science and society, and an outline of emerging areas of research. Key themes addressed include the way genomic based DNA technologies have become incorporated into diverse arenas of clinical practice and research whilst also extending beyond the clinic; the role of genomics in contemporary bioeconomies; how challenges in the governance of medical genomics can both reconfigure and stabilise regulatory processes and jurisdictional boundaries; how questions of diversity and justice are situated across different national and transnational terrains of genomic research; and how genomics informs and is shaped by developments in fields such as epigenetics, synthetic biology, stem cell, microbial and animal model research. Presenting cutting edge research from leading social science scholars, the Handbook provides a unique and important contribution to the field. It brings a rich and varied cross disciplinary social science perspective that engages with both the history and contemporary context of genomics and post-genomics, and considers the now global and transnational terrain in which these developments are unfolding."--Provided by publisher.
Sociology --- Social policy --- Genetics --- Social medicine --- E-books --- Medical care --- Medical sociology --- Medicine --- Medicine, Social --- National planning --- State planning --- Social theory --- Social aspects --- Public health --- Public welfare --- Medical ethics --- Medical sociologists --- Biology --- Embryology --- Mendel's law --- Adaptation (Biology) --- Breeding --- Chromosomes --- Heredity --- Mutation (Biology) --- Variation (Biology) --- Economic policy --- Family policy --- Social history --- Social sciences --- Society & social sciences --- Medical genetics --- Genomics --- Genome research --- Genomes --- Molecular genetics --- Clinical genetics --- Diseases --- Heredity of disease --- Human genetics --- Medical sciences --- Pathology --- Genetic disorders --- Research --- Genetic aspects --- genomics --- developing economies --- Africa --- Brazil --- Haplotype --- Senegal --- Sickle cell disease --- Genomics. --- Genetics, Medical. --- Genetic Testing. --- Bioethical Issues. --- Génomique --- Génétique médicale --- Société.
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