CLINICAL GENETICS & GENOMIC MEDICINE : A Practical Guide to Inherited Disorders, DNA Testing, Variant Interpretation, Counseling, and Precision Therapy
Language: English
Published by Independently Published Jun 2026, 2026
- Softcover
- New
Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH
AbeBooks seller since August 14, 2006
Condition: New
£ 237.31
Quantity: 2 available
Add to basketItem description from seller
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.…
Seller Inventory # 9798181248366
- Title
- CLINICAL GENETICS & GENOMIC MEDICINE : A Practical Guide to Inherited Disorders, DNA Testing, Variant Interpretation, Counseling, and Precision Therapy
- Author
- Gilberto Grey Emmerich
- Publisher
- Independently Published Jun 2026
- Publication year
- 2026
- Condition
- Neu
- Binding
- Taschenbuch
- Language
- English
- ISBN 13
- 9798181248366
- Item weight
- 1,037 grams
- Dimensions
- 279x216x23 mm
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.
Use it as a reference companion for deeper study, case-based learning, and more confident navigation of genomic medicine concepts.
"Synopsis" may belong to another edition of this title.
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