A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region
- 1 March 1998
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 53 (3), 226-227
- https://doi.org/10.1111/j.1399-0004.1998.tb02683.x
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23Human Molecular Genetics, 1997
- A tetranucleotide repeat polymorphism within the human elastin gene (ELNi1)Clinical Genetics, 1997
- Identification of Genes from a 500-kb Region at 7q11.23 That Is Commonly Deleted in Williams Syndrome PatientsGenomics, 1996
- LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive CognitionCell, 1996
- Assignment of the human and mouse LIM-kinase genes (LIMK1; Limk1) to chromosome bands 7q11.23 and 5G1, respectively, by in situ hybridizationCytogenetic and Genome Research, 1996
- Hemizygosity at the elastin locus in a developmental disorder, Williams syndromeNature Genetics, 1993
- Natural history of Williams syndrome: Physical characteristicsThe Journal of Pediatrics, 1988