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Методы генетики человека в медицине

Студенческие работы

American Psychiatric Publishing, 2005. — 155 p. Research Advances in Genetics and Genomics: Implications for Psychiatry introduces mental health professionals to exciting breakthroughs in endophenotypes, animal models, microarrays, and genetic mapping, as well as general strategies for identifying the genetic mechanisms of mental illnesses. Uniquely valuable both as summary and...
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Academic Press, 2001. — 384 p. — (Advances in Genetics Volume 44). Tay-Sachs disease is a rare hereditary disease caused by a genetic mutation that leaves the body unable to produce an enzyme necessary for fat metabolism in nerve cells, producing central nervous system degeneration. In infants, it is characterized by progressive mental deterioration, blindness, paralysis,...
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Springer, 2014. — 233 p. Preimplantation genetic diagnosis (PGD) is a rapidly advancing field of reproductive genetics. With the significant improvements achieved over the last few years in the understanding of many genetic diseases and in the techniques of molecular genetic testing, new genetic diseases are being added to the list of conditions amenable to PGD almost on a weekly...
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London: Routledge, 2008. — 403 p. With the first patent being granted to “BiDil,” a combined medication that is deemed to be most effective for a specific “race,” African-Americans for a specific form of heart failure, the on-going debate about the effect of the older category of race has been renewed. What role should “race” play in the discussion of genetic alleles and...
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Springer, 2014. — 132 p. In the past four years, many genetic loci have been implicated for BMI from the outcomes of genome-wide association studies (GWAS), primarily in adults. Insulin-induced gene 2 (INSIG2) was the first locus to be reported by this method to have a role in obesity but replication attempts have yielded inconsistent outcomes. The identification of the second...
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2nd EEdition. — Springer Publishing Company, LLC, 2016. — 531 p. — ISBN 0826129129. Completely updated to help nurses learn to think genetically Today's nurses must be able to think genetically to help individuals and families who are affected by genetic disease or contemplating genetic testing. This book is a classic resource for nursing students and practitioners at all levels...
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CRC Press, 2014. — 324 p. Based on one leading center’s experience with over 100,000 cases, the new edition of this extensively illustrated atlas provides a detailed manual for procedures and techniques in preimplantation genetic diagnosis. New topics in this edition include de novo mutations, diseases with genetic predisposition, and HLA typing. The book provides insight from...
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3rd Edition. — Springer, 2005. — 587 p. — ISBN 082612366X. Designated a Doody's Core Title! The third edition of this award-winning text provides new and updated knowledge about genetics issues relevant to nursing practice. Read in sequence or used as a reference, this is a comprehensive overview of how genetics affetcs the care that nurses provide. In addition to a summary of...
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Springer, 2014. — 201 p. This book focus on genetic diagnostics for Uniparental Disomy (UPD), a chromosomal disorder defined by the exceptional presence of a chromosome pair derived from only one parent, which leads to a group of rare diseases in humans. First the molecular and cytogenetic background of UPD is described in detail; subsequently, all available information of the...
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Oxford University Press, 2014. — 305 p. The book is an online resource devoted to research methodology in genetic counseling. It offers step-by-step guidance for conducting research, from the development of a question to the publication of findings. Genetic counseling examples and practical tips guide readers through the research and publication processes. With a highly...
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Springer, 2014. — 274 p. One aim of this atlas is to present a comprehensive overview of limb malformation phenotypes in order to provide the clinician with a tool that facilitates the diagnostic process. With the enormous advances in molecular and developmental biology, the genetic basis of many limb malformations and their relationship to each other has been elucidated. Thus, a...
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Academic Press, 2014. — 207 p. Between the Lines of Genetic Code lays out methodologies and tools for the measurement and evaluation of gene-gene and gene-environment studies and gives perspective on the future of this discipline. The book begins by defining terms for interaction studies, describing methodologies, and critically assessing the viability of current study designs...
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Academic Press, 2015. — 1465 p. The book provides a comprehensive introduction and reference to the foundations and key practical aspects relevant to the majority of neurologic and psychiatric disease. A favorite of over three generations of students, clinicians and scholars, this new edition retains and expands the informative, concise and critical tone of the first edition....
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Белянина С.И., Кузьмина К.А., Андронова Т.А., Боброва Л.А., Сигарева Л.Е., Сергеева И.В. Методическое пособие. – Саратов: Изд-во СМИ, 2001. – 64 с. Методическое пособие предназначено для самостоятельной работы студентов I курса лечебного, педиатрического, стоматологического факультетов медицинских ВУЗов, а также студентов по специальности "Сестринское дело" при изучении...
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Белянина С.И., Кузьмина К.А., Андронова Т.А., Боброва Л.А., Сигарева Л.Е., Сергеева И.В. СМИ, 1997. – 40 с. Методические рекомендации предназначены для самостоятельной внеаудиторной подготовки к занятиям и экзамену студентов I курса лечебного, педиатрического, стоматологического факультетов, а также для студентов по специальности "Сестринское дело" при изучении раздела...
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Пермь: Книжный формат, 2013. — 222 с. Рассмотрены особенности гигиенической индикации цитогенетических наруше- ний при воздействии химических факторов с мутагенной активностью. Представлены комплексы маркеров экспозиции и маркеров эффектов, их критериальные параметры в условиях устойчивого воздействия химических мутагенов как факторов риска развития цитогенетических нарушений и...
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М.: Медицинское информационное агентство, 2002. — 591 с.: ил. — ISBN 5-89481-100-7. Монография посвящена современным возможностям ДНК-диагностики и основанного на ней медико-генетического консультирования при наследственных заболеваниях нервной системы. Авторами обобщен большой собственный опыт в данной области исследований в сопоставлении с результатами аналогичных работ,...
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Учебное пособие для вузов. - Воронеж: Изд-во ВГУ, 2008. - 46 с. Учебное пособие подготовлено на кафедре генетики, цитологии и биоинженерии биолого-почвенного факультета Воронежского государственного университета. В пособии рассматриваются два метода исследования генетики человека: клинико-генеалогический и популяционно-статистический. Представлены теоретические аспекты...
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