View in EDS

Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening.

Saved in:
Bibliographic Details
Title: Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening.
Authors: Handt M; Faculty of Health, Witten/Herdecke University, Alfred-Herrhausen-Straße 50, 58448 Witten, Germany., Epplen A; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany., Hoffjan S; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany., Mese K; Faculty of Health, Witten/Herdecke University, Alfred-Herrhausen-Straße 50, 58448 Witten, Germany., Epplen JT; Faculty of Health, Witten/Herdecke University, Alfred-Herrhausen-Straße 50, 58448 Witten, Germany; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany., Dekomien G; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany. Electronic address: gabriele.dekomien@rub.de.
Source: Molecular and cellular probes [Mol Cell Probes] 2014 Oct-Dec; Vol. 28 (5-6), pp. 279-83. Date of Electronic Publication: 2014 Aug 27.
Publication Type: Journal Article
Journal Info: Publisher: Academic Press Country of Publication: England NLM ID: 8709751 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-1194 (Electronic) Linking ISSN: 08908508 NLM ISO Abbreviation: Mol Cell Probes Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1096-1194
DOI:10.1016/j.mcp.2014.08.003