Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker
- 1 January 1989
- Vol. 4 (1) , 110-111
- https://doi.org/10.1016/0888-7543(89)90323-6
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Mapping of mutation causing Friedreich's ataxia to human chromosome 9Nature, 1988
- Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S15)Nucleic Acids Research, 1987
- A human single-copy DNA probe (DR 47) detects a Taq I RFLP on chromosome 9 (D9S5)Nucleic Acids Research, 1987
- Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosomeHuman Genetics, 1986
- The Quebec Cooperative Study of Friedreich's Ataxia: 1974-1984 — 10 Years of ResearchCanadian Journal of Neurological Sciences, 1984
- Friedreich's Ataxia in the South of Italy : A Clinical and Biochemical Survey of 23 PatientsCanadian Journal of Neurological Sciences, 1980
- Clinical Description and Roentgenologic Evaluation of Patients with Friedreich's AtaxiaCanadian Journal of Neurological Sciences, 1976
- Friedreich's ataxia in Western NorwayClinical Genetics, 1975