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List of works by Cherif Beldjord

A T to G mutation in the polypyrimidine tract of the second intron of the human beta-globin gene reduces in vitro splicing efficiency: evidence for an increased hnRNP C interaction

scientific article

A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11

scientific article

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

scientific article

ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation

scientific article (publication date: 15 April 2002)

CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy

scientific article

Cloning and characterization of the human V3 pituitary vasopressin receptor

scientific article

Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22

scientific article

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)

scientific article

Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria

scientific article

Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation

scientific article

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

scientific article

Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54)

scientific article (publication date: 30 July 1999)

So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation

scientific article (publication date: June 2002)

doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)

scientific article

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