Craniofacial characteristics of fragile X syndrome in mouse and man

European Journal of Human Genetics

Volumn 21, Issue 8, 2013, Pages 816-823

  Heulens, Inge ^a   Suttie, Michael ^b   Postnov, Andrei ^a   De Clerck, Nora ^a   Perrotta, Concetta S ^a   Mattina, Teresa ^c   Faravelli, Francesca ^d   Forzano, Francesca ^d   Frank Kooy, R ^a   Hammond, Peter ^b  

^a UNIVERSITY OF ANTWERP   (Belgium)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY OF CATANIA   (Italy)

^d Medical Genetics Unit   (Italy)

Author keywords

Craniofacial features; Dense surface modelling; fmr1 KO mouse; Fragile X syndrome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CARTILAGE; CHILD; CLINICAL ARTICLE; COGNITIVE DEFECT; COMPUTER ASSISTED TOMOGRAPHY; CRANIOFACIAL MALFORMATION; EYE; FACE GROWTH; FACIES; FEMALE; FRAGILE X SYNDROME; GENE MUTATION; HUMAN; MALE; MANDIBLE; MEDICAL PHOTOGRAPHY; MOUSE; NASAL BONE; NEUROANATOMY; NONHUMAN; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SKULL;

ADOLESCENT; ADULT; ANIMALS; CHILD; CHILD, PRESCHOOL; CRANIOFACIAL ABNORMALITIES; DISEASE MODELS, ANIMAL; FEMALE; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; HUMANS; MALE; MANDIBLE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MIDDLE AGED; MODELS, ANATOMIC; MUTATION; SKULL; X-RAY MICROTOMOGRAPHY; YOUNG ADULT;

ANIMALIA;

EID: 84880920687     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2012.265     Document Type: Article

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