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Abnormal Skeletal Phenotypes

Overview of attention for book
Cover of 'Abnormal Skeletal Phenotypes'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Skull
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    Chapter 2 Thorax
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    Chapter 3 Spine
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    Chapter 4 Pelvis
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    Chapter 5 Long Bones
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    Chapter 6 Hands
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    Chapter 7 Feet
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    Chapter 8 Joints
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    Chapter 9 Generalized Skeletal Abnormalities
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    Chapter 10 Aarskog Syndrome
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    Chapter 11 Achondrogenesis, Type IB
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    Chapter 12 Achondrogenesis, Type II
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    Chapter 13 Achondroplasia
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    Chapter 14 Acrofacial Dysostosis, Nager Type
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    Chapter 15 Angelman Syndrome
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    Chapter 16 Apert Syndrome
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    Chapter 17 Asphyxiating Thoracic Dysplasia
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    Chapter 18 Atelosteogenesis
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    Chapter 19 Bardet-Biedl Syndrome
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    Chapter 20 Beckwith-Wiedemann Syndrome
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    Chapter 21 C Syndrome
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    Chapter 22 Campomelic Dysplasia
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    Chapter 23 Carpenter Syndrome
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    Chapter 24 Cerebro-costo-mandibular Syndrome
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    Chapter 25 CHARGE Association
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    Chapter 26 Chondrodysplasia Punctata, Conradi-Hünermann Type
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    Chapter 27 Chondrodysplasia Punctata, Rhizomelic Type
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    Chapter 28 Chondrodysplasia Punctata, Brachytelephalangic Type
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    Chapter 29 Chondroectodermal Dysplasia
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    Chapter 30 Chromosome 4p- Syndrome
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    Chapter 31 Chromosome Trisomy 13 Syndrome
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    Chapter 32 Chromosome Trisomy 18 Syndrome
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    Chapter 33 Chromosome Trisomy 21 Syndrome
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    Chapter 34 Cleidocranial Dysplasia
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    Chapter 35 Cockayne Syndrome
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    Chapter 36 Coffin-Lowry Syndrome
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    Chapter 37 Coffin-Siris Syndrome
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    Chapter 38 Cohen Syndrome
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    Chapter 39 Craniometaphyseal Dysplasia, Dominant Type
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    Chapter 40 Cri-du-chat Syndrome
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    Chapter 41 Crouzon Syndrome
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    Chapter 42 De Lange Syndrome
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    Chapter 43 Diaphyseal Dysplasia
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    Chapter 44 Diastrophic Dysplasia
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    Chapter 45 Dubowitz Syndrome
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    Chapter 46 Dyschondrosteosis
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    Chapter 47 Dysosteosclerosis
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    Chapter 48 Ectodermal Dysplasias
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    Chapter 49 Ehlers-Danlos Syndromes
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    Chapter 50 Enchondromatosis
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    Chapter 51 Exostoses, Multiple
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    Chapter 52 Fanconi Anemia
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    Chapter 53 Focal Dermal Hypoplasia Syndrome
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    Chapter 54 Freeman-Sheldon Syndrome
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    Chapter 55 Frontometaphyseal Dysplasia
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    Chapter 56 Goldenhar Syndrome
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    Chapter 57 Hallermann-Streiff Syndrome
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    Chapter 58 Holt-Oram Syndrome
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    Chapter 59 Kenny-Caffey Syndrome
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    Chapter 60 Klippel-Feil Anomaly
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    Chapter 61 Klippel-Trenaunay-Weber Syndrome
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    Chapter 62 Kniest Dysplasia
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    Chapter 63 Larsen Syndrome
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    Chapter 64 Marfan Syndrome
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    Chapter 65 McCune-Albright Syndrome
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    Chapter 66 Meckel Syndrome
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    Chapter 67 Melnick-Needles Syndrome
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    Chapter 68 Melorheostosis
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    Chapter 69 Mental Retardation, X-Linked, Associated with FRA Xq27.3
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    Chapter 70 Mesomelic Dwarfism, Langer Type
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    Chapter 71 Mesomelic Dwarfism, Nievergelt Type
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    Chapter 72 Metatropic Dysplasia
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    Chapter 73 Multiple Epiphyseal Dysplasia
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    Chapter 74 Nail-Patella Syndrome
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    Chapter 75 Nevoid Basal Cell Carcinoma Syndrome
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    Chapter 76 Noonan Syndrome
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    Chapter 77 Opitz Syndrome
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    Chapter 78 Oro-facio-digital Syndrome, Type I
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    Chapter 79 Oro-facio-digital Syndrome, Type II
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    Chapter 80 Osteogenesis Imperfecta, Type I
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    Chapter 81 Osteogenesis Imperfecta, Type IIA
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    Chapter 82 Osteogenesis Imperfecta, Type IIB/III
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    Chapter 83 Osteopathia Striata with Cranial Sclerosis
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    Chapter 84 Osteopetrosis, Infantile Type
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    Chapter 85 Osteopetrosis, Adult Type
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    Chapter 86 Osteopoikilosis
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    Chapter 87 Oto-palato-digital Syndrome, Type I
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    Chapter 88 Oto-palato-digital Syndrome, Type II
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    Chapter 89 Pena-Shokeir Syndrome
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    Chapter 90 Pfeiffer Syndrome
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    Chapter 91 Poland Syndrome
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    Chapter 92 Prader-Willi Syndrome
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    Chapter 93 Progeria
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    Chapter 94 Pseudoachondroplasia
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    Chapter 95 Pyknodysostosis
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    Chapter 96 Roberts Syndrome
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    Chapter 97 Robin Sequence
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    Chapter 98 Robinow Syndrome
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    Chapter 99 Rubinstein-Taybi Syndrome
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    Chapter 100 Saethre-Chotzen Syndrome
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    Chapter 101 Seckel Syndrome
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    Chapter 102 Short Rib-Polydactyly Syndrome, Type I
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    Chapter 103 Short Rib-Polydactyly Syndrome, Type II
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    Chapter 104 Silver-Russell Syndrome
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    Chapter 105 Smith-Lemli-Opitz Syndrome
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    Chapter 106 Sotos Syndrome
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    Chapter 107 Spondyloepimetaphyseal Dysplasia, Irapa Type
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    Chapter 108 Spondyloepimetaphyseal Dysplasia, Strudwick Type
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    Chapter 109 Spondyloepiphyseal Dysplasia Congenita
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    Chapter 110 Spondyloepiphyseal Dysplasia Tarda
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    Chapter 111 Spondylometaphyseal Dysplasia, Kozlowski Type
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    Chapter 112 Stickler Syndrome
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    Chapter 113 Thanatophoric Dysplasia
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    Chapter 114 Thrombocytopenia-Absent Radius Syndrome
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    Chapter 115 Treacher-Collins Syndrome
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    Chapter 116 Tricho-rhino-phalangeal Syndrome, Type I
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    Chapter 117 Tricho-rhino-phalangeal Syndrome, Type II
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    Chapter 118 Turner Syndrome
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    Chapter 119 VATER Association
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    Chapter 120 Williams Syndrome
Attention for Chapter 40: Cri-du-chat Syndrome
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Chapter title
Cri-du-chat Syndrome
Chapter number 40
Book title
Abnormal Skeletal Phenotypes
Published by
Springer, Berlin, Heidelberg, January 2005
DOI 10.1007/3-540-30361-8_40
Book ISBNs
978-3-54-067997-4, 978-3-54-030361-9
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 2 20%
Unknown 8 80%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 20%
Unknown 8 80%