FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome
Top Cited Papers
- 19 June 2008
- journal article
- case report
- Published by Elsevier in American Journal of Human Genetics
- Vol. 83 (1) , 89-93
- https://doi.org/10.1016/j.ajhg.2008.05.015
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett‐like featuresAmerican Journal of Medical Genetics Part A, 2008
- Integration of Smad and Forkhead Pathways in the Control of Neuroepithelial and Glioblastoma Cell ProliferationCell, 2004
- Multiplex Ligation-Dependent Probe Amplification (MLPA) Detects Large Deletions in the MECP2 Gene of Swedish Rett Syndrome PatientsGenetic Testing, 2003
- Rett syndrome in adolescent and adult females: Clinical and molecular genetic findingsAmerican Journal of Medical Genetics Part A, 2003
- Human PLU-1 Has Transcriptional Repression Properties and Interacts with the Developmental Transcription Factors BF-1 and PAX9Journal of Biological Chemistry, 2003
- An update on clinically applicable diagnostic criteria in Rett syndromeEuropean Journal of Paediatric Neurology, 2002
- Brain Factor-1Controls the Proliferation and Differentiation of Neocortical Progenitor Cells through Independent MechanismsJournal of Neuroscience, 2002
- Rett syndrome in Spain: mutation analysis and clinical correlationsBrain & Development, 2001
- The Winged-Helix Protein Brain Factor 1 Interacts with Groucho and Hes Proteins To Repress TranscriptionMolecular and Cellular Biology, 2001
- Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.Human Molecular Genetics, 2000