The Authors declare no conflict of interest.
Neurofibromatosis type 1 in two siblings due to maternal germline mosaicism
Version of Record online: 27 MAY 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 85, Issue 4, pages 386–389, April 2014
How to Cite
Trevisson, E., Forzan, M., Salviati, L. and Clementi, M. (2014), Neurofibromatosis type 1 in two siblings due to maternal germline mosaicism. Clinical Genetics, 85: 386–389. doi: 10.1111/cge.12177
- Issue online: 10 MAR 2014
- Version of Record online: 27 MAY 2013
- Accepted manuscript online: 26 APR 2013 12:09PM EST
- Manuscript Revised: 18 APR 2013
- Manuscript Accepted: 18 APR 2013
- Manuscript Received: 21 FEB 2013
|cge12177-sup-0001-FigureS1.pdf||PDF document||378K||Figure S1. PCR-RFLP assay by HpaII digestion of the 222 bp fragment of NF1 exon 12 amplified from serial dilutions of mutant Pt2 DNA mixed with wild type-DNA. The percentage of the mutant DNA is indicated.|
|cge12177-sup-0002-FigureS2.pdf||PDF document||378K||Figure S2. Sequence analyses of the 222 bp fragment of NF1 exon 12 amplified from serial dilutions of mutant Pt2 DNA mixed with wild type-DNA. The percentage of the mutant DNA is indicated. The arrows indicate the position of the mutation.|
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