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POLYMORPHIC DNA MARKERS IN PRENATAL DIAGNOSIS OF FRAGILE X SYNDROME

✍ Scribed by Oberle, I; Mandel, J.L; Boué, J; Mattei, M.G; Mattei, J.F

Book ID
123225302
Publisher
The Lancet
Year
1985
Tongue
English
Weight
151 KB
Volume
325
Category
Article
ISSN
0140-6736

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## Abstract Linkage analysis using the polymorphic loci DXS369, DXS296, DXS297 and DXS306 was carried out on a cohort of 17 families segregating for fragile X syndrome. The observed recombination fractions at: DXS369 (Zmax = 3. 02; theta=0. 06), DXS297 (Zmax= 2. 92; theta = 0.0), DXS296 (Zmax = 3.

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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