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Human Molecular Genetics|July 1, 1996
Identification by STS PCR screening of a microdeletion in Xp21.3-22.1 associated with non-specific mental retardationP Billuart, M C Vinet, V des Portes, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1979
Structural bases of the inhibitory effects of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin SR L Nagel, R M Bookchin, J Johnson, et al.Neurology|October 14, 2005
Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasiaG Zanni, Y Saillour, M Nagara, et al.American Journal of Medical Genetics|July 12, 1996
X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pterV des Portes, L Bachner, T Brüls, et al.Tissue Antigens|July 30, 2002
Two novel CD1 E alleles identified in black African individualsR Tamouza, R Sghiri, R Ramasawmy, et al.Neurogenetics|October 20, 2005
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosisK Poirier, D Lacombe, B Gilbert-Dussardier, et al.European Journal of Human Genetics : EJHG|March 1, 1997
Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardationT Bienvenu, H Der-Sarkissian, P Billuart, et al.Cell|March 7, 1998
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndromeV des Portes, J M Pinard, P Billuart, et al.Journal of Pediatric Hematology/Oncology|July 1, 1997
Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. The French Study Group on Sickle Cell DiseaseM de Montalembert, M Belloy, F Bernaudin, et al.Human Molecular Genetics|June 9, 1998
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)V des Portes, F Francis, J M Pinard, et al.Pageof 20