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Self-assessment Questions for Clinical Molecular Genetics

Autor Haiying Meng
en Limba Engleză Paperback – 28 mai 2019
Review Questions of Clinical Molecular Genetics presents a comprehensive study guide for the board and certificate exams presented by the American College of Medical Genetics and Genomics (ACMG) and the American Board of Medical Genetics and Genomics (ABMGG). It provides residents and fellows in genetics and genomics with over 1,000 concise questions, ranging from topics in cystic fibrosis, to genetic counseling, to trinucleotide repeat expansion disorders. It puts key points in the form of questions, thus challenging the reader to retain knowledge. As board and certificate exams require knowledge of new technologies and applications, this book helps users meet that challenge.


  • Includes over 1,0000 multiple-choice, USMLE style questions to help readers prepare for specialty exams in Clinical Cytogenetics and Clinical Molecular Genetics
  • Designed to assist clinical molecular genetic fellows, genetic counselors, medical genetic residents and fellows, and molecular pathologist residents in preparing for their certification exam
  • Assists trainees on how to follow guidelines and put them in practice
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Specificații

ISBN-13: 9780128099674
ISBN-10: 0128099674
Pagini: 816
Dimensiuni: 216 x 276 x 39 mm
Greutate: 1.86 kg
Editura: ELSEVIER SCIENCE

Public țintă

Clinical geneticists in training (clinical molecular genetic follows, clinical cytogenetic fellows, clinical biochemistry fellows); Medical genetic residents/fellows, Pathology residents/fellows (molecular pathology, laboratory medicine), Genetic counselor students.

Cuprins

1. ACMGG Guidelines, CAP Checklists2. Connective Tissue and Skeletal Diseases3. Cystic Fibrosis4. General Molecular Genetic Knowledge5. Genetic Counseling6. Hematological Disorders7. Hereditary Cancer Syndromes8. Lysosomal Storage Disorders9. Metabolic disorders10. Molecular Genetics in Malignancies11. Molecular Genetic Nomenclatures12. Neuromuscular Disorders13. Other Common Genetic syndromes14. Pharmacogenetics15. Trinucleotide Repeat Expansion Disorders