When neuropediatrics meets odontology

Neuropediatrics

Volumn 38, Issue 2, 2007, Pages 57-58

  Bloch Zupan, A ^a,b,c,d,e  

^a UNIVERSITÉ DE STRASBOURG   (France)

^b UNIVERSITY HOSPITAL OF STRASBOURG   (France)

^c INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^d CNRS   (France)

^e UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMELOGENESIS IMPERFECTA; ATAXIA; BRAIN MALFORMATION; DISEASE ASSOCIATION; EDITORIAL; GENETIC ASSOCIATION; HUMAN; NEUROLOGY; ODONTOLOGY; PEDIATRICS; PHENOTYPE; PRIORITY JOURNAL; RUBINSTEIN SYNDROME; TOOTH DEVELOPMENT; TOOTH MALFORMATION;

ATAXIA; BRAIN DISEASES; CHILD; HUMANS; MYELIN SHEATH; ODONTOGENESIS; TOOTH ABNORMALITIES;

EID: 34548716454     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-985135     Document Type: Editorial

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