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| Foreword To The Second Edition | |
| Foreword To The First Edition | |
| Preface | |
| Introduction | |
| Aarskog Syndrome | |
| Achondroplasia | |
| Alagille Syndrome | |
| Albinism and Hermansky-Pudlak Syndrome | |
| Angelman Syndrome | |
| Arthrogryposis | |
| ATR-X | |
| Bardet-Biedl Syndrome | |
| Beckwith-Wiedemann Syndrome and Hemihyperplasia | |
| CHARGE Association | |
| Coffin-Lowry Syndrome | |
| Cornelia de Lange Syndrome | |
| Costello Syndrome | |
| Craniosynostosis Syndromes | |
| Deletion 22q13 Syndrome (Phelan-McDermid Syndrome) | |
| Denys-Drash and Frasier Syndromes | |
| Down Syndrome | |
| Ehlers-Danlos Syndromes | |
| Fetal Alcohol Syndrome and Fetal Alcohol Spectrum Disorder | |
| Fetal Anticonvulsant Syndrome | |
| Fragile X Syndrome | |
| Gorlin Syndrome (Nevoid Basal Cell Carcinoma Syndrome) | |
| Hereditary Hemorrhagic Telangiectasia | |
| Holoprosencephaly | |
| Incontinentia Pigmenti | |
| Kabuki Syndrome | |
| Klinefelter Syndrome | |
| Marfan Syndrome | |
| Myotonic Dystrophy Type 1 | |
| Neurofibromatosis Type 1 | |
| Noonan Syndrome | |
| Oculo-Auriculo-Vertebral Spectrum | |
| Osteogenesis Imperfecta | |
| Pallister-Hall and Greig Cephalopolysyndactyly Syndromes | |
| Prader-Willi Syndrome | |
| Proteus Syndrome | |
| Rett Syndrome | |
| Robin Sequence | |
| Rubinstein-Taybi Syndrome | |
| Russell-Silver Syndrome | |
| Smith-Lemli-Opitz Syndrome | |
| Smith-Magenis Syndrome | |
| Sotos Syndrome | |
| Stickler Syndrome | |
| Treacher Collins Syndrome | |
| Trisomy 18 and Trisomy 13 Syndromes | |
| Tuberous Sclerosis | |
| Turner Syndrome | |
| VATER Association | |
| Velo-Cardio-Facial Syndrome | |
| Von Hippel-Lindau Syndrome | |
| WAGR Syndrome | |
| Williams Syndrome | |
| Wolf-Hirschhorn (4p-) Syndrome | |
| Index | |
| Table of Contents provided by Publisher. All Rights Reserved. |
