Mosaic DCX deletion causes subcortical band heterotopia in males.

Quélin, Chloé; Saillour, Yoann; Souville, Isabelle; Poirier, Karine; N'guyen-Morel, Marie Ange; Vercueil, Laurent; Millisher-Bellaiche, Anne Elodie; Boddaert, Nathalie; Dubois, Fanny; Chelly, Jamel; Beldjord, Cherif; Bahi-Buisson, Nadia

Quélin, Chloé; Saillour, Yoann; Souville, Isabelle; Poirier, Karine; N'guyen-Morel, Marie Ange; Vercueil, Laurent; Millisher-Bellaiche, Anne Elodie; Boddaert, Nathalie; Dubois, Fanny; Chelly, Jamel; Beldjord, Cherif; Bahi-Buisson, Nadia.

Affiliation

Quélin C; Génétique Clinique Centre de référence "Maladies Rares" CLAD-Ouest CHU Rennes, Rennes, France.

Neurogenetics ; 13(4): 367-73, 2012 Nov.

Article in En | MEDLINE | ID: mdl-22833188

Subject(s)

Classical Lissencephalies and Subcortical Band Heterotopias/genetics; Gene Deletion; Microtubule-Associated Proteins/genetics; Mosaicism; Neuropeptides/genetics; Child, Preschool; Chromosomes, Human, X/genetics; Classical Lissencephalies and Subcortical Band Heterotopias/diagnosis; Classical Lissencephalies and Subcortical Band Heterotopias/diagnostic imaging; Doublecortin Domain Proteins; Doublecortin Protein; Exons; Humans; Magnetic Resonance Imaging; Male; Prenatal Diagnosis; Ultrasonography, Prenatal

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neuropeptides / Gene Deletion / Classical Lissencephalies and Subcortical Band Heterotopias / Microtubule-Associated Proteins / Mosaicism Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Child, preschool / Humans / Male Language: En Journal: Neurogenetics Journal subject: GENETICA / NEUROLOGIA Year: 2012 Type: Article Affiliation country: France

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