Jean-Louis Mandel: Difference between revisions
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[[File:Jean-Louis Mandel par Claude Truong-Ngoc mai 2013.jpg|thumb|Jean-Louis Mandel]] |
[[File:Jean-Louis Mandel par Claude Truong-Ngoc mai 2013.jpg|thumb|Jean-Louis Mandel]] |
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'''Jean-Louis Mandel''' (born 12 February 1946) is French physician and geneticist. In 1994 he won the [[Richard Lounsbery Award]] for |
'''Jean-Louis Mandel''' (born 12 February 1946) is [[French people|French]] [[physician]] and [[geneticist]]. In 1994, he won the [[Richard Lounsbery Award]] for his work in [[human genetics]], in particular his discovery of the [[genetic mutation|mutation]] of [[fragile X Syndrome]]. The mutation has since been found at the origin of the disease.<ref>[http://www.nasonline.org/programs/awards/richard-lounsbery-award.html Richard Lounsbery Award.] National Academy of Sciences. Retrieved 6 September 2017.</ref> |
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== References == |
== References == |
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Revision as of 15:07, 18 November 2018
Jean-Louis Mandel (born 12 February 1946) is French physician and geneticist. In 1994, he won the Richard Lounsbery Award for his work in human genetics, in particular his discovery of the mutation of fragile X Syndrome. The mutation has since been found at the origin of the disease.[1]
References
- ^ Richard Lounsbery Award. National Academy of Sciences. Retrieved 6 September 2017.
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