A new RFLP with StuI and probe cX55.7 (DXS105) and its usefulness in carrier analysis of fragile X syndrome.

Rekilä A M, Väisänen M L, Kähkönen M, Leisti J, Winqvist R

Department of Clinical Genetics, Oulu University Central Hospital, Finland.

Hum Genet. 1988 Oct;80(2):193. doi: 10.1007/BF00702869.

Abstract

The authors report on a new RFLP at DXS105 suitable for carrier detection of fragile X syndrome.

摘要

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