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Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers

✍ Scribed by Yuji Takemoto; Tetsuro Miki; Jun Nakura; Kumi Nishikawa; Kouzin Kamino; Shunichi Takeda; Kogo Kuzu; Mitsuhiro Osame; Masanori Nakagawa; Itsuro Higuchi; Takeshi Yamada; Tetsuya Takayanagi; Shiro Matsubara; Kyoko Saita; Shin-ichiro Takai; Tasuku Honjo; Toshio Ogihara

Book ID: 105393841
Publisher: Nature Publishing Group
Year: 1989
Tongue: English
Weight: 326 KB
Volume: 34
Category: Article
ISSN: 1435-232X
DOI: 10.1007/bf01900720

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Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome

✍ S. N. Thibodeau; H. R. Dorkins; K. R. Faulk; R. Berry; A. C. M. Smith; R. Hagerm 📂 Article 📅 1988 🏛 Springer 🌐 English ⚖ 939 KB

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