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Publication | Open Access

The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males

DOIFull Paper Access

100

Citations

35

References

2006

Year

Stephen R.F. Twigg, Kazuya Matsumoto, Alexa Kidd, Anne Goriely, Indira B. Taylor, Richard B. Fisher, A. Jeannette M. Hoogeboom, Irene M.J. Mathijssen, Maria Teresa Cruz Lourenço, Jenny E.V. Morton,
The American Journal of Human Genetics

References

YearCitations

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