Human Genetics: From Molecules to Medicine provides balanced coverage of molecular and clinical genetics for the preclinical medical student with rele ...
A comprehensive review of the recent developments in DNA repair research that have potential for translational applications. The book explains in deta ...
In this thoroughly revised and expanded third edition of the highly praised classic, The Principles of Clinical Cytogenetics, a panel of hands-on expe ...
Timing, racing, combating, struggling and targeting are some actions through which cellular fate could be reflected and evaluated. Interaction between ...
Congenital hip disease (CHD) is the main cause of secondary osteoarthritis (OA) of the hip in young adults, which accounts for almost 40% of all cases ...
اختلال هماهنگی رشدی (developmental coordination disorder) یا DCD که به عنوان دیسپراکسی یا دیسپراکسیای رشد و نموی (dyspraxia) نیز نامیده می شود، با عنو ...
Over the past several decades the incidence of autism spectrum disorders (ASD) has increased dramatically. the etiology of ASD remains an unsolved puz ...
Alexia - Diagnosis, Treatment and Theory This book is a comprehensive review of the main acquired disorders of reading: hemianopic, pure and cent ...
This text collates and examines the jurisprudence that currently exists in respect of blood-tied genetic connection, arguing that the right to identit ...
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously ...
Protein Misfolding Disorders - A Trip into the ER Neurodegenerative disorders such as Amyotrophic lateral sclerosis (ALS), Alzheimer’s disease (A ...
This extensively illustrated reference work is designed for health professionals who care for newborn infants including neonatologists, pediatricians, ...
This Brief provides a concise review of chaperonopathies, i.e., diseases in which molecular chaperones play an etiologic-pathogenic role. Introductory ...
Over the last decade there has been a substantial increase in our understanding of the genetic basis of common disorders such as stroke. Stroke Geneti ...
What happens with our genome and epigenome in the first fundamental days of our development? How can this be analysed? What do we need to know when fa ...
Am I My Genes? - Confronting Fate and Family Secrets in the Age of Genetic Testing In the fifty years since DNA was discovered, we have seen extrao ...
This book introduces readers to Next Generation Sequencing applications in medical genetics. The authors discuss the direct application of next-genera ...
Human Genetic Diversity - Functional Consequences for Health and Disease This book describes the remarkable progress which has been made in defin ...
Rationality and the Genetic Challenge - Making People Better Should we make people healthier, smarter, and longer-lived if genetic and medical ad ...
A complete introductory text on how to integrate basic genetic principles into the practice of clinical medicine. Medical Genetics is the first text t ...
Investigating the Human Genome - Insights into Human Variation and Disease Susceptibility An Up-to-Date Assessment of Recent Advances in Human Ge ...
Uniparental Disomy (UPD) in Clinical Genetics - A Guide for Clinicians and Patients This book focus on genetic diagnostics for Uniparental Disomy ...
Genes, Memes, Culture, and Mental Illness - Toward an Integrative Model What produces mental illness: genes, environment, both,neither? The answe ...
Handbook on Analyzing Human Genetic Data - Computational Approaches and Software This handbook offers guidance on selections of appropriate compu ...
In Fragile X-Associated Tremor Ataxia Syndrome (FXTAS), the editors present information on all aspects of FXTAS, including clinical features and curre ...
