European Gene Mapping Project (EUROGEM): Breakpoint panels for human chromosomes based on the CEPH reference families
- 1 November 1996
- journal article
- Published by Wiley in Annals of Human Genetics
- Vol. 60 (6), 447-486
- https://doi.org/10.1111/j.1469-1809.1996.tb01614.x
Abstract
No abstract availableKeywords
This publication has 53 references indexed in Scilit:
- Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis regionHuman Molecular Genetics, 1995
- Integrated human genome–wide maps constructed using the CEPH reference panelNature Genetics, 1994
- CEPH Consortium Map of Chromosome 9Genomics, 1994
- A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellitesHuman Molecular Genetics, 1993
- The CEPH Consortium Linkage Map of Human Chromosome 13Genomics, 1993
- Characterization of a DNA Sequence Family in the Prader-Willi/Angelman Syndrome Chromosome Region in 15q11-q13Genomics, 1993
- A cyclophilin-related protein involved in the function of natural killer cells.Proceedings of the National Academy of Sciences, 1993
- The CEPH consortium linkage map of human chromosome 15qGenomics, 1992
- An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndromeNature, 1992
- Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genomeGenomics, 1990