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Perinatal Genetics

Buch | Softcover
206 Seiten
2019
Elsevier - Health Sciences Division (Verlag)
978-0-323-53094-1 (ISBN)
CHF 129,95 inkl. MwSt
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Get a quick, expert overview of the fast-changing field of perinatal genetics with this concise, practical resource. Drs. Mary Norton, Jeffrey A. Kuller, and Lorraine Dugoff fully cover the clinically relevant topics that are key to providers who care for pregnant women and couples contemplating pregnancy. It's an ideal resource for Ob/Gyn physicians, maternal-fetal medicine specialists, and clinical geneticists, as well as midwives, nurse practitioners, and other obstetric providers.



Provides a comprehensive review of basic principles of medical genetics and genetic counseling, molecular genetics, cytogenetics, prenatal screening options, chromosomal microarray analysis, whole exome sequencing, prenatal ultrasound, diagnostic testing, and more.
Contains a chapter on fetal treatment of genetic disorders.
Consolidates today's available information and experience in this important area into one convenient resource.

Dr. Mary Norton is a Maternal Fetal Medicine specialist as well as a clinical geneticist. She specializes in the care of women at high risk for having a baby with a birth defect or genetic disorder. She oversees the prenatal diagnosis program at UCSF and is an expert in high-risk obstetrical ultrasound and prenatal diagnosis procedures such as amniocentesis and CVS. Her research interests include the use of new genetic technologies for fetal testing, and she is a national expert in the use of cell free DNA testing. She also has a particular interest in patient attitudes and preferences regarding prenatal testing.

Preface 1. Principles of Medical Genetics and Genomics

2. Non-Mendelian Genetics

3. Principles of Genetic Counseling

4. Cytogenetics: Part 1, General Concepts and Aneuploid Conditions

5. Cytogenetics: Part 2, Structural Rearrangements and Reproductive Impact

6. Molecular Genetics

7. Carrier Screening

8. Serum and Ultrasound Based Screening Tests for Aneuploidy

9. Cell Free DNA Screening

10. Ultrasound Markers for Aneuploidy

11. Genetic Evaluation of Fetal Sonographic Abnormalities

12. Chromosomal Microarray Analysis

13. Exome and Genome Sequencing

14. Prenatal Diagnostic Testing

15. Preimplantation Genetic Screening and Diagnosis

16. Fetal Treatment of Genetic Disorders

Erscheinungsdatum
Verlagsort Philadelphia
Sprache englisch
Maße 191 x 235 mm
Gewicht 450 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Gynäkologie / Geburtshilfe
Medizin / Pharmazie Medizinische Fachgebiete Pädiatrie
Studium 2. Studienabschnitt (Klinik) Humangenetik
ISBN-10 0-323-53094-X / 032353094X
ISBN-13 978-0-323-53094-1 / 9780323530941
Zustand Neuware
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