PDF Diagnosis & Treatment of the Unborn Child: PDF

by Maria I. New

Ch. 1. Carrier screening for multiple diseases in the Ashkenazi Jewish Community: a model for future prenatal genetic screening and disease prevention —
Ch. 2. Hemophilia problems in carrier identification and fetal diagnosis —
Ch. 3. Fragile X syndrome —
Ch. 4. Fanconi anemia —
Ch. 5. Inherited variation in susceptibility to cancer in the unborn child —
Ch. 6. The RSH syndrome: paradigmatic metabolic malformation syndrome? —
Ch. 7. Diagnosis of osteogenesis imperfecta and potentials for therapy —
Ch. 8. Skeletal dysplasias —
Ch. 9. Muscular dystrophies Ch. 10. Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiency —
Ch. 11. Prenatal diagnosis and treatment in congenital adrenal hyperplasia —
Ch. 12. Intrauterine diagnosis/carrier detection for disorders of the androgen receptor —
Ch. 13. Fetal and neonatal malnutrition —
Ch. 14. Preimplantation genetic diagnosis (PGD): challenges and potentials —
Ch. 15. Uniparental disomy —
Ch. 16. Recovering fetal cells in maternal blood for prenatal genetic diagnosis and thalassemia Ch. 17. Fetal cells in maternal circulation to diagnose hemoglobinopathies and thalassemia —
Ch. 18. Overview of fetal therapy and subcutaneous surgery —
Ch. 19. Hematopoietic stem cell transplantation: delivery techniques —
Ch. 20. Preimplantation genetic diagnosis (PGD) —
Ch. 21. Ethical considerations in fetal therapy —
Ch. 22. New obligations of physicians in genetics —
Ch. 23. Cloning and ethics.

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Book Title
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PublisherIdelson-Gnocchi Ltd. Publishing
Pages count185
eBook formatHardcover, (torrent)En
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