Abnormal Skeletal Phenotypes From Simple Signs to Complex Diagnoses /
When one is asked to review a manuscript in order of the different parts of the skeleton and comprises to write a foreword,one always asks oneself,“Is there about 600 pages. anything special about this book?”“Does it supply The reader will ?nd something about the in- us with unique information?”I he...
| Κύριοι συγγραφείς: | , |
|---|---|
| Συγγραφή απο Οργανισμό/Αρχή: | |
| Μορφή: | Ηλεκτρονική πηγή Ηλ. βιβλίο |
| Γλώσσα: | English |
| Έκδοση: |
Berlin, Heidelberg :
Springer Berlin Heidelberg,
2005.
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| Θέματα: | |
| Διαθέσιμο Online: | Full Text via HEAL-Link |
Πίνακας περιεχομένων:
- I
- Skull
- Thorax
- Spine
- Pelvis
- Long Bones
- Hands
- Feet
- Joints
- Generalized Skeletal Abnormalities
- II
- Aarskog Syndrome
- Achondrogenesis, Type IB
- Achondrogenesis, Type II
- Achondroplasia
- Acrofacial Dysostosis, Nager Type
- Angelman Syndrome
- Apert Syndrome
- Asphyxiating Thoracic Dysplasia
- Atelosteogenesis
- Bardet-Biedl Syndrome
- Beckwith-Wiedemann Syndrome
- C Syndrome
- Campomelic Dysplasia
- Carpenter Syndrome
- Cerebro-costo-mandibular Syndrome
- CHARGE Association
- Chondrodysplasia Punctata, Conradi-Hünermann Type
- Chondrodysplasia Punctata, Rhizomelic Type
- Chondrodysplasia Punctata, Brachytelephalangic Type
- Chondroectodermal Dysplasia
- Chromosome 4p- Syndrome
- Chromosome Trisomy 13 Syndrome
- Chromosome Trisomy 18 Syndrome
- Chromosome Trisomy 21 Syndrome
- Cleidocranial Dysplasia
- Cockayne Syndrome
- Coffin-Lowry Syndrome
- Coffin-Siris Syndrome
- Cohen Syndrome
- Craniometaphyseal Dysplasia, Dominant Type
- Cri-du-chat Syndrome
- Crouzon Syndrome
- De Lange Syndrome
- Diaphyseal Dysplasia
- Diastrophic Dysplasia
- Dubowitz Syndrome
- Dyschondrosteosis
- Dysosteosclerosis
- Ectodermal Dysplasias
- Ehlers-Danlos Syndromes
- Enchondromatosis
- Exostoses, Multiple
- Fanconi Anemia
- Focal Dermal Hypoplasia Syndrome
- Freeman-Sheldon Syndrome
- Frontometaphyseal Dysplasia
- Goldenhar Syndrome
- Hallermann-Streiff Syndrome
- Holt-Oram Syndrome
- Kenny-Caffey Syndrome
- Klippel-Feil Anomaly
- Klippel-Trenaunay-Weber Syndrome
- Kniest Dysplasia
- Larsen Syndrome
- Marfan Syndrome
- McCune-Albright Syndrome
- Meckel Syndrome
- Melnick-Needles Syndrome
- Melorheostosis
- Mental Retardation, X-Linked, Associated with FRA Xq27.3
- Mesomelic Dwarfism, Langer Type
- Mesomelic Dwarfism, Nievergelt Type
- Metatropic Dysplasia
- Multiple Epiphyseal Dysplasia
- Nail-Patella Syndrome
- Nevoid Basal Cell Carcinoma Syndrome
- Noonan Syndrome
- Opitz Syndrome
- Oro-facio-digital Syndrome, Type I
- Oro-facio-digital Syndrome, Type II
- Osteogenesis Imperfecta, Type I
- Osteogenesis Imperfecta, Type IIA
- Osteogenesis Imperfecta, Type IIB/III
- Osteopathia Striata with Cranial Sclerosis
- Osteopetrosis, Infantile Type
- Osteopetrosis, Adult Type
- Osteopoikilosis
- Oto-palato-digital Syndrome, Type I
- Oto-palato-digital Syndrome, Type II
- Pena-Shokeir Syndrome
- Pfeiffer Syndrome
- Poland Syndrome
- Prader-Willi Syndrome
- Progeria
- Pseudoachondroplasia
- Pyknodysostosis
- Roberts Syndrome
- Robin Sequence
- Robinow Syndrome
- Rubinstein-Taybi Syndrome
- Saethre-Chotzen Syndrome
- Seckel Syndrome
- Short Rib-Polydactyly Syndrome, Type I
- Short Rib-Polydactyly Syndrome, Type II
- Silver-Russell Syndrome
- Smith-Lemli-Opitz Syndrome
- Sotos Syndrome
- Spondyloepimetaphyseal Dysplasia, Irapa Type
- Spondyloepimetaphyseal Dysplasia, Strudwick Type
- Spondyloepiphyseal Dysplasia Congenita
- Spondyloepiphyseal Dysplasia Tarda
- Spondylometaphyseal Dysplasia, Kozlowski Type
- Stickler Syndrome
- Thanatophoric Dysplasia
- Thrombocytopenia-Absent Radius Syndrome
- Treacher-Collins Syndrome
- Tricho-rhino-phalangeal Syndrome, Type I
- Tricho-rhino-phalangeal Syndrome, Type II
- Turner Syndrome
- VATER Association
- Williams Syndrome.
