Polymicrogyria in a child with inv dup del(9p) and 22q11.2 microduplication

Author:

Mosca A.L.,Callier P.,Faivre L.,Marle N.,Mejean N.,Thauvin-Robinet C.,Masurel-Paulet A.,Madinier N.,Durand C.,Couillaud G.,Ragot S.,Huet F.,Teyssier J.R.,Mugneret F.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference40 articles.

1. 1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features;Alberti;Clin Genet,2007

2. Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation;Alkan;Genet Couns,2002

3. Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions;Bearden;Cereb Cortex,2008

4. Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion;Chen;Prenat Diagn,2002

5. Hydrocephalus, microcephaly, and neuronal migrational abnormalties: A 15-year mystery explained by a 6q deletion;Curry;Proc Greenwood Genet Center,2000

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