A high-resolution genetic linkage map of the pericentromeric region of the human X chromosome
Open Access
- 1 March 1995
- Vol. 26 (1) , 39-46
- https://doi.org/10.1016/0888-7543(95)80080-6
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Integrated human genome–wide maps constructed using the CEPH reference panelNature Genetics, 1994
- Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage mapNature Genetics, 1994
- Primers for the dinucleotide repeat at the DXS453 locus also recognizes the DXS983 locusHuman Molecular Genetics, 1993
- Isolation and Characterization of Three Microsatellite Markers in the Proximal Long Arm of the Human X ChromosomeGenomics, 1993
- Characterization of Microsatellite Polymorphisms DXS691 and DXS692: Genetic Mapping to Xq26.2-Xq27 and Xq25-Xq26.2Genomics, 1993
- Abnormal Segregation of Alleles in CEPH Pedigree DNAs Arising from Allele Loss in Lymphoblastoid DNAGenomics, 1993
- The gene for aarskog syndrome is located between DXS255 and DXS566 (Xp11.2–Xq13)Genomics, 1992
- An 18-locus linkage map of the pericentromeric region of the human X chromosome: Genetic framework for mapping X-linked disordersGenomics, 1991
- Efficient computation of lod scores: genotype elimination, genotype redefinition, and hybrid maximum likelihood algorithmsAnnals of Human Genetics, 1989
- THE ESTIMATION OF MAP DISTANCES FROM RECOMBINATION VALUESAnnals of Eugenics, 1943