Linkage data, using the polymorphic markers 52A (DXS51), F9, 4D-8 (DXS98), and St14 (DXS52), are presented from 14 fragile X pedigrees and from 7 normal pedigrees derived from the collection of the Centre d't~tude du Polymorphisme Humaine. A multipoint linkage analysis indicates that the most probab
Linkage homogeneity near the fragile X locus in normal and fragile X families
✍ Scribed by Suthers, G.K.; Mulley, J.C.; Voelckel, M.A.; Dahl, N.; Väisänen, M.L.; Steinbach, P.; Glass, I.A.; Schwartz, C.E.; van Oost, B.A.; Thibodeau, S.N.; Haites, N.E.; Oostra, B.A.; Schinzel, A.; Carballo, M.; Morris, C.P.; Hopwood, J.J.; Sutherland, G.R.
- Book ID
- 121770349
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 856 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0888-7543
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Linkage data using the markers F9 (factor IX), DXS15 (DX131, and DXS134 (cpX67) are presented from 26 pedigrees segregating with fragile X (fra[XI) syndrome. Cytogenetic and DNA data were combined in 2-point linkage analysis for the estimation of lod scores and carrier probabilities in potential car
## Letter to in Norma To the Editor: the Editor: Fragile X Chromosome Males I found the recent report by Hecht, Jacky, and Sutherland [1982] on the Fragile X Chromosome Workshop (Jerusalem, September 198 1) particularly interesting and a good summary, it seems, of the present situation. However, I