Contribution of VANGL2 mutations to isolated neural tube defects.

Kibar, Z; Salem, S; Bosoi, C M; Pauwels, E; De Marco, P; Merello, E; Bassuk, A G; Capra, V; Gros, P

Kibar, Z; Salem, S; Bosoi, C M; Pauwels, E; De Marco, P; Merello, E; Bassuk, A G; Capra, V; Gros, P.

Affiliation

Kibar Z; Department of Obstetrics and Gynecology, CHU Sainte Justine Research Center and University of Montreal, Montreal, Quebec, Canada. zoha.kibar@recherche-stejustine.qc.ca

Clin Genet ; 80(1): 76-82, 2011 Jul.

Article in En | MEDLINE | ID: mdl-20738329

Subject(s)

Intracellular Signaling Peptides and Proteins/genetics; Membrane Proteins/genetics; Neural Tube Defects/genetics; Amino Acid Sequence; Female; Genetic Predisposition to Disease; Humans; Male; Molecular Sequence Data; Mutation; Mutation, Missense; Neural Tube Defects/pathology

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intracellular Signaling Peptides and Proteins / Membrane Proteins / Neural Tube Defects Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Clin Genet Year: 2011 Type: Article Affiliation country: Canada

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