We invite you to read an interesting paper recently published on the European Journal of Human Genetics: “9q33.3q34.11 microdeletion: new contiguous gene syndrome encompassing STXBP1, LMX1B and ENG genes […]
Molecular investigations, CGH-Array, Molecular karyotype, Intellectual disability, Epilepsy
Am J Med Genet A. – 2014 Nov 25 Authors Nizon M1, Andrieux J, Rooryck C, de Blois MC, Bourel-Ponchel E, Bourgois B, Boute O, David A, Delobel B, Duban-Bedu B, Giuliano F, Goldenberg A, Grotto S,Héron D, Karmous-Benailly […]
Molecular investigations, CGH-Array, Molecular karyotype, Human cytogenetic, Intellectual disability, Epilepsy, Precocious puberty, Language delay
Microgenomics Staff invites you to read an interesting paper on CNVs and epilepsy, recently published by a group of American colleagues in the European Journal […]
Molecular investigations, CGH-Array, Molecular karyotype, Postnatal diagnosis, Epilepsy, Microdeletions
