CNS malformations: Gene locations of known human mutations

European Journal of Paediatric Neurology

Volumn 9, Issue 6, 2005, Pages 427-431

  Sarnat, Harvey B ^a  

^a UNIVERSITY OF CALGARY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL INHERITANCE; CENTRAL NERVOUS SYSTEM MALFORMATION; CHROMOSOME 10Q; CHROMOSOME 11P; CHROMOSOME 13Q; CHROMOSOME 17P; CHROMOSOME 18P; CHROMOSOME 1P; CHROMOSOME 1Q; CHROMOSOME 2Q; CHROMOSOME 3P; CHROMOSOME 5Q; CHROMOSOME 6Q; CHROMOSOME 7Q; CHROMOSOME 9Q; CHROMOSOME XP; CHROMOSOME XQ; GENE LOCUS; GENE MUTATION; HUMAN; PRIORITY JOURNAL;

CENTRAL NERVOUS SYSTEM; GENES; HUMANS; MUTATION;

EID: 29644444482     PISSN: 10903798     EISSN: 15322130     Source Type: Journal    
DOI: 10.1016/j.ejpn.2005.06.005     Document Type: Article

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