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Contents |
Ch. 1. Introduction -- Ch. 2. Achondroplasia -- Ch. 3. Angelman Syndrome -- Ch. 4. Beckwith-Wiedemann Syndrome -- Ch. 5. CHARGE Association -- Ch. 6. Cornelia de Lange Syndrome -- Ch. 7. Down Syndrome -- Ch. 8. The Ehlers-Danlos Syndromes -- Ch. 9. Fetal Alcohol Syndrome -- Ch. 10. Fragile X Syndrome -- Ch. 11. Incontinentia pigmenti -- Ch. 12. Klinefelter Syndrome -- Ch. 13. Marfan Syndrome -- Ch. 14. Neurofibromatosis Type 1 -- Ch. 15. Noonan Syndrome -- Ch. 16. Oculo-auriculo-vertebral spectrum -- Ch. 17. Osteogenesis imperfecta -- Ch. 18. Prader-Willi Syndrome -- Ch. 19. Robin sequence -- Ch. 20. Russell-Silver Syndrome |
Contents |
Ch. 21. Smith-Lemli-Opitz Syndrome -- Ch. 22. Smith-Magenis Syndrome -- Ch. 23. Sotos Syndrome -- Ch. 24. Stickler Syndrome -- Ch. 25. Trisomy 18 and Trisomy 13 Syndromes -- Ch. 26. Tuberous sclerosis -- Ch. 27. Turner Syndrome -- Ch. 28. VATER Association -- Ch. 29. Velo-cardio-facial Syndrome -- Ch. 30. Williams Syndrome |
Bibliography note | Includes bibliographical references and index. |
LCCN | 00038213 |
ISBN | 047131286X : |