A Fifth Locus for Bardet-Biedl Syndrome Maps to Chromosome 2q31
- 1 March 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (3) , 900-904
- https://doi.org/10.1086/302301
Abstract
No abstract availableThis publication has 72 references indexed in Scilit:
- Genetic Heterogeneity of Bardet–Biedl Syndrome in a Distinct Canadian Population: Evidence for a Fifth LocusGenomics, 1999
- A practical diagnostic test for choroideremiaOphthalmology, 1998
- Diverse Mutations in the Gene for Cartilage Oligomeric Matrix Protein in the Pseudoachondroplasia–Multiple Epiphyseal Dysplasia Disease SpectrumAmerican Journal of Human Genetics, 1998
- Chromosome 3p14 Homozygous Deletions and Sequence Analysis of FRA3BHuman Molecular Genetics, 1997
- The molecular basis of fragile sites in human chromosomesCurrent Opinion in Genetics & Development, 1995
- Human genome organizationCurrent Opinion in Genetics & Development, 1995
- The Cardinal Manifestations of Bardet–Biedl Syndrome, a Form of Laurence–Moon–Biedl SyndromeNew England Journal of Medicine, 1989
- Inbreeding in outport NewfoundlandAmerican Journal of Medical Genetics, 1988
- Psoriasis of early and late onset: Characterization of two types of psoriasis vulgarisJournal of the American Academy of Dermatology, 1985
- X-linked retinitis pigmentosa.British Journal of Ophthalmology, 1975