Epstein's inborn errors of development : the molecular basis of clinical disorders of morphogenesis /
Epstein's Inborn Errors of Development provides essays on pathways of development and thoughtful reviews of dysmorphic syndromes for which the causative gene has been identified. It is a top-to-bottom revision of the landmark text that both revolutionized and accelerated the field of human gene...
Clasificación: | Libro Electrónico |
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Otros Autores: | , |
Formato: | Electrónico eBook |
Idioma: | Inglés |
Publicado: |
Oxford ; New York :
Oxford University Press,
[2016]
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Edición: | Third edition. |
Colección: | Oxford monographs on medical genetics ;
no. 67. |
Temas: | |
Acceso en línea: | Texto completo |
Tabla de Contenidos:
- Series ; Untitled; Epstein's Inborn Errors of€Development ; Copyright ; Contents ; Contributors ; I. GENERAL CONCEPTS ; 1. Human Malformations and Their Genetic Basis ; 2. Principles of Differentiation and Morphogenesis ; 3. Model Organisms in the Study of Development and Disease.
- 4. Human Genomics and Human Development II. Patterns of Development ; 5. Development of Left-. Right Asymmetry ; 6. Neural Crest Formation and Craniofacial Development ; 7. Development of the Nervous System ; 8. Development of the Eye ; 9. Development of the Ear.
- 10. Molecular Regulation of Cardiogenesis 11. Update on the Development of the Vascular System and Its Sporadic Disorders ; 12. Muscle and Somite Development ; 13. The Development of Bone and Cartilage ; 14. Limb Development ; 15. The Sex-. Determination Pathway.
- 16. Development of the Kidney 17. Development of the Endodermal Derivatives in Lung, Liver, Pancreas, and Gut ; 18. Development of Epidermal Appendages:€Teeth and Hair ; III. Defined Core Developmental Pathways Linked to€Cilia ; A: Ciliary Functions:€Genesis, Transport, and Reabsorbtion.
- 19. Primary Ciliary Dyskinesia (Kartagener Syndrome) 20. The Molecular Basis of Joubert Syndrome and Related Disorders ; 21. The Bardet-. Biedl Syndrome ; 22. The Molecular Basis of Oral-. Facial-. Digital Type I€Syndrome ; 23. Meckel Syndrome.