Delineation of the Critical Interval of Bardet-Biedl Syndrome 1 (BBS1) to a Small Region of 11q13, through Linkage and Haplotype Analysis of 91 Pedigrees
- 31 December 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (6) , 1672-1679
- https://doi.org/10.1086/302684
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- A Founder Effect in the Newfoundland Population Reduces the Bardet-Biedl Syndrome I (BBS1) Interval to 1 cMAmerican Journal of Human Genetics, 1999
- A Fifth Locus for Bardet-Biedl Syndrome Maps to Chromosome 2q31American Journal of Human Genetics, 1999
- A 2.8-Mb Clone Contig of the Multiple Endocrine Neoplasia Type 1 (MEN1) Region at 11q13Genomics, 1997
- A Sequence-Ready High-Resolution Physical Map of the Best Macular Dystrophy Gene Region in 11q12–q13Genomics, 1997
- Phenotypic differences among patients with Bardet‐Biedl syndrome linked to three different chromosome lociAmerican Journal of Medical Genetics, 1995
- Bardet–Biedl syndrome is linked to DNA markers on chromosome 11 q and is genetically heterogeneousNature Genetics, 1994
- Linkage of Bardet–Biedl syndrome to chromosome 16q and evidence for non–allelic genetic heterogeneityNature Genetics, 1993
- Mapping recessive ophthalmic diseases: Linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1qGenomics, 1990
- Bardet‐Biedl and Laurence‐Moon syndromes in a mixed Arab populationClinical Genetics, 1988
- Linkage analysis and family classification under heterogeneityAnnals of Human Genetics, 1983