Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22
- 1 July 1989
- Vol. 5 (1) , 144-148
- https://doi.org/10.1016/0888-7543(89)90099-2
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localizationClinical Genetics, 1988
- A primary genetic map of the pericentromeric region of the human X chromosomeGenomics, 1988
- Two different genes for X-linked retinitis pigmentosaGenomics, 1988
- Molecular heterogeneity of translocations associated with muscular dystrophyClinical Genetics, 1987
- A Sequence in M13 Phage Detects Hypervariable Minisatellites in Human and Animal DNAScience, 1987
- Characterization and use of somatic cell hybrids with interspecific translocations involving the human X chromosomeAnnals of Human Genetics, 1987
- Report of the committee on the genetic constitution of the X and Y chromosomesCytogenetic and Genome Research, 1987
- Inherited Chondrodysplasia Punctata Due to a Deletion of the Terminal Short Arm of an X ChromosomeNew England Journal of Medicine, 1984
- Viability of λ phages carrying a perfect palindrome in the absence of recombination nucleasesNature, 1983
- The macronuclear ribosomal DNA of Tetrahymena pyriformis is a palindromeJournal of Molecular Biology, 1976