Serveur d'exploration sur les relations entre la France et l'Australie - Analysis (UK)

Index « Auteurs » - entrée « Stephen Robertson »
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Stephen Richards < Stephen Robertson < Stephen Rogerson  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 2.
Ident.Authors (with country if any)Title
001F35 (2012) Tiziana Pisano [Italie] ; A. James Barkovich [États-Unis] ; Richard J. Leventer [Australie] ; Waney Squier [Royaume-Uni] ; Ingrid E. Scheffer [États-Unis, Australie] ; Elena Parrini [Italie] ; Susan Blaser [Canada] ; Carla Marini [Italie] ; Stephen Robertson [Nouvelle-Zélande] ; Gaetano Tortorella [Italie] ; Felix Rosenow [Allemagne] ; Pierre Thomas [France] ; George Mcgillivray [Australie] ; Eva Andermann [Canada] ; Frederick Andermann [Canada] ; Samuel F. Berkovic [États-Unis] ; William B. Dobyns [États-Unis] ; Renzo Guerrini [Italie]Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis
002241 (2011) Matthew L. Warman [États-Unis] ; Valerie Cormier-Daire [France] ; Christine Hall [Royaume-Uni] ; Deborah Krakow [États-Unis] ; Ralph Lachman [États-Unis] ; Martine Lemerrer [France] ; Geert Mortier [Belgique] ; Stefan Mundlos [Allemagne] ; Gen Nishimura [Japon] ; David L. Rimoin [États-Unis] ; Stephen Robertson [Nouvelle-Zélande] ; Ravi Savarirayan [Australie] ; David Sillence [Australie] ; Juergen Spranger [Allemagne] ; Sheila Unger [Allemagne, Suisse] ; Bernhard Zabel [Allemagne] ; Andrea Superti-Furga [Allemagne, Suisse]Nosology and classification of genetic skeletal disorders: 2010 revision

List of associated KwdEn.i

Nombre de
documents
Descripteur
1Acanthosis nigricans
1Achondrogenesis type
1Acrofacial dysostosis
1Activity subunit
1Aggrecan
1Aggrecan group
1American journal
1Anomaly
1Asphyxiating thoracic dysplasia
1Atelosteogenesis type
1Autosomal
1Autosomal recessive
1Autosomal recessive form
1Binding protein
1Birth defects orig artic
1Blomstrand dysplasia
1Bone
1Bone cysts
1Bone density group
1Brachydactyly
1Brachydactyly type
1Cartilaginous exostoses
1Cation channel
1Cdags syndrome
1Cerebellum
1Child health
1Chloride channel
1Chondrodysplasia punctata
1Chst3 type
1Classification
1Cleidocranial dysplasia
1Collagen
1Collagen group
1Constitutional bone diseases
1Constitutional diseases
1Constitutional disorders
1Corpus callosum
1Craniofrontonasal syndrome
1Craniometaphyseal dysplasia
1Craniosynostosis
1Defect
1Density lipoprotein protein
1Desbuquois dysplasia
1Diagnostic process
1Different genes
1Differentiation factor
1Disorder
1Disorder inheritance
1Disorganized development
1Dysostoses
1Dysostosis
1Dysplasia
1Dysplasia society
1Dysplasia syndrome type
1Dysplasia type
1Dysplasias group
1Eiken dysplasia
1Epiphyseal
1Feet syndrome
1Fgfr2
1Fgfr2 mutations
1Fgfr3
1Fibroblast
1Fibroblast growth factor receptor
1Filamin
1Form type
1Gdf5
1Gdf5 growth
1Gene
1Genet
1Genet part
1Genetic basis
1Genetic disease
1Genetic heterogeneity
1Genetic osteoarthropathies
1Genetics
1Geroderma osteodysplasticum
1Gli3 family member
1Greenberg dysplasia
1Haar syndrome
1Heavy chain
1Hedgehog
1Homeobox
1Hospitalier universitaire vaudois
1Howard hughes
1Hypertrophic osteoarthropathy
1Hypophosphatemic
1Hypophosphatemic rickets
1Imperfecta
1Inclusion criteria
1Individual disorders
1Infantile
1Infantile form
1Infantile forms
1Intermediate form
1International nomenclature
1Jansen dysplasia
1Joint formation
1Lausanne
1Limb defects

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