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Self-assessment questions for clinical molecular genetics /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Meng, Haiying (Autor)
Formato: Electrónico eBook
Idioma:Inglés
Publicado: London, United Kingdom : Academic Press, an imprint of Elsevier, 2019.
Temas:
Acceso en línea:Texto completo

MARC

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100 1 |a Meng, Haiying,  |e author. 
245 1 0 |a Self-assessment questions for clinical molecular genetics /  |c Haiying Meng. 
264 1 |a London, United Kingdom :  |b Academic Press, an imprint of Elsevier,  |c 2019. 
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500 |a Includes index. 
588 0 |a Online resource; title from PDF title page (ScienceDirect, viewed June 4, 2019). 
505 0 |a Front Cover; Self-assessment Questions for Clinical Molecular Genetics; Copyright Page; Dedication; Contents; About the Author; Preface; Reference; Further Reading; Acknowledgments; 1 General Molecular Genetic Knowledge; Questions; Answers; References; Further Reading; 2 Regulations From Oversight Agencies; Laboratory Accreditation Bodies; Consumer Protection Agencies; Professional Licensing Organizations; Other Regulatory Bodies; Questions; Answers; References; Further Reading; 3 Molecular Genetic Nomenclature; Questions; Answers; References; 4 Disorders of Unstable Repeat Sequences 
505 8 |a QuestionsAnswers; References; Further Reading; 5 Cystic Fibrosis; Questions; Answers; References; Additional Resources; 6 Nonneoplastic Hematological Disorders; Questions; Answers; References; 7 Oncology-Constitutional; Proto-Oncogenes Versus Tumor Suppressor Genes; Hereditary Cancer Predisposition Syndrome and Knudson's Two-Hit Hypothesis; Chromosome Breakage Syndromes; Founder Effect in Ashkenazi Jewish; Questions; Answers; References; 8 Oncology-Acquired; Primary and Secondary Genetic Aberrations in Oncogenesis/Tumorigenesis/Carcinogenesis; Clonality, Clonal Expansion, and Clonal Evolution 
505 8 |a Tumor HeterogeneityLoss of Heterozygosity; Samples for Genetic Tests; Questions; Answers; References; 9 Lysosomal Storage Disorders; Questions; Answers; References; Further Reading; 10 Neuromuscular Disorders; Questions; Answers; References; Further Reading; 11 Prenatal, Newborn Screen, and Metabolic Disorders; Questions; Answers; References; Further Reading; 12 Other Common Genetic Syndromes; Questions; Answers; References; Further Reading; 13 Pharmacogenetics; Questions; Answers; References; Further Reading; 14 Genetic Counseling-Introduction; Questions; Answers; References; Further Reading 
650 0 |a Molecular genetics  |x Examinations  |v Study guides. 
650 2 |a Molecular Biology  |0 (DNLM)D008967 
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