Genomic medicine practical guide (2 Ergebnisse)

Buch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - The field of Molecular Diagnostics is rapidly evolving and molecular characterization of neoplasms is becoming an increasingly important part of the pathologic work up and diagnosis of many tumor types. This work provides a high-yield reference book that compiles critical information related to molecular biomarkers for various solid tumor and hematologic malignancy subtypes. It is succinct yet comprehensive enough to be suitable for fellows in training and medical professionals with an interest in molecular pathology and biomarkers. The book covers many aspects of molecular diagnostics, from techniques to applications and comprehensive summaries of the current molecular biomarkers of critical importance in solid and liquid tumors. Attention is also specifi cally devoted to bioinformatics and next generation sequencing, as well as pre-analytical issues that must be considered for accurate interpretation of molecular results in the context of overall patient care.This text focuses on clinical utility and validity and serves as an 'owner's manual' in Genomic Diagnostics for the practicing pathologist, pathology fellows and residents and other health care providers. Physicians will find this book invaluable as a quick reference for current molecular testing modalities and guidelines, tumor board preparation, deciding which test to order and interpreting genomic laboratory results. In addition, it is an accessible for trainees as a board review preparation reference.…

Taschenbuch. Zustand: Neu. Neuware - Turn complex hereditary disease, laboratory reports, and genomic decision-making into a clearer clinical learning pathway. Clinical Genetics & Genomic Medicine is a comprehensive professional reference for readers who need a structured way to understand modern human heredity, molecular diagnosis, cytogenetics, variant classification, disease recognition, pharmacogenomics, reproductive applications, and emerging genomic interventions. Designed for genetics fellows, senior residents, clinicians, medical learners, and healthcare educators, this atlas-style resource moves from foundational molecular principles to practical organ-system applications. It connects DNA structure, inheritance patterns, chromosome analysis, sequencing platforms, ACMG/AMP evidence logic, genetic counseling, ethical issues, and precision therapeutics into one organized learning framework. The manuscript is arranged as a broad clinical atlas, beginning with molecular foundations and pedigree reasoning before moving into cytogenetics, chromosomal disorders, genomic test selection, variant classification, organ-system genetics, prenatal and reproductive applications, pharmacogenomics, gene therapy, genome editing, counseling practice, and ethical decision-making. Its structure supports careful study, professional review, and classroom or clinical teaching. Inside, you will find: - Build a stronger foundation in molecular biology, inheritance patterns, pedigree analysis, and chromosomal abnormalities.- Understand how sequencing, cytogenetics, microarray, exome, genome, and emerging technologies support diagnostic reasoning.- Apply structured thinking to variant classification, VUS communication, cascade screening, and family-risk assessment.- Explore major areas of medical genomics, including metabolic, neurogenetic, cardiovascular, skeletal, cancer, renal, immune, dermatologic, prenatal, and pharmacogenomic conditions.- Connect molecular findings with careful clinical interpretation, patient communication, surveillance planning, and multidisciplinary care.- Review ethical, counseling, consent, confidentiality, and service-delivery issues that shape responsible genomic practice.Whether you are studying, teaching, reviewing clinical genetics, or building confidence with genomic reports, this book offers a detailed and organized pathway through one of the fastest-evolving areas of modern healthcare.Use it as a reference companion for deeper study, case-based learning, and more confident navigation of genomic medicine concepts.…