A YAC Contig in Xq22.3–q23, fromDXS287toDXS8088, Spanning the Brain-Specific Genesdoublecortin(DCX) andPAK3
- 1 September 1998
- Vol. 52 (2) , 214-218
- https://doi.org/10.1006/geno.1998.5424
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly SyndromeCell, 1998
- Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24American Journal of Medical Genetics, 1997
- 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.Journal of Medical Genetics, 1997
- Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosomeGene, 1997
- Regional localization of two non-specific X-linked mental retardation genes (MRX30 andMRX31)American Journal of Medical Genetics, 1996
- Localisation of two candidate genes for mental retardation using a YAC physical map of the Xq21.1-21.2 subbands.Journal of Medical Genetics, 1996
- Refined Mapping and YAC Contig Construction of the X-Linked Cleft Palate and Ankyloglossia Locus (CPX) Including the Proximal X–Y Homology Breakpoint within Xq21.3Genomics, 1996
- A YAC contig map of the human genomePublished by Cold Spring Harbor Laboratory ,1995
- Band heterotopia: Correlation of outcome with magnetic resonance imaging parametersAnnals of Neurology, 1994
- Causal heterogeneity in isolated lissencephalyNeurology, 1992