Homozygosity Mapping in Families with Joubert Syndrome Identifies a Locus on Chromosome 9q34.3 and Evidence for Genetic Heterogeneity
- 1 December 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (6) , 1666-1671
- https://doi.org/10.1086/302655
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Joubert’s syndrome: new cases and review of clinicopathologic correlationPediatric Neurology, 1999
- Follow-Up in Children with Joubert SyndromeNeuropediatrics, 1997
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- Genomic Structure and Chromosomal Localization of the Mouse LIM/Homeobox Gene Lhx3Genomics, 1995
- Mechanisms of Neural Patterning and Specification in the Development CerebellumAnnual Review of Neuroscience, 1995
- Avoiding Recomputation in Linkage AnalysisHuman Heredity, 1994
- Joubert syndrome: A reviewAmerican Journal of Medical Genetics, 1992
- Swaying is a mutant allele of the proto-oncogene Wnt-1Published by Elsevier ,1991
- Linkage probability and its approximate confidence interval under possible heterogeneityGenetic Epidemiology, 1986
- Joubert Syndrome: Episodic Hyperpnea, Abnormal Eye Movements, Retardation and Ataxia, Associated with Dysplasia of the Cerebellar VermisNeuropediatrics, 1977