Zobrazeno 1 - 1
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pro vyhledávání: '"Célia Delozier-Blanchet"'
Autor:
Sandra Blumenfeld, I. Oberlé, Niels Tommerup, Célia Delozier-Blanchet, Dominique Heitz, Marie Françoise Croquette, Carl Birger van der Hagen, François Rousseau, Jean-Louis Mandel, Valérie Biancalana, Pierre Jalbert, Simon Gilgenkrantz, Christine Kretz, Marie-Antoinette Voelckel, Joelle Boué
Publikováno v:
The New England journal of medicine. 325(24)
The fragile X syndrome, the most common form of inherited mental retardation, is caused by mutations that increase the size of a specific DNA fragment of the X chromosome (in Xq27.3). Affected persons have both a full mutation and abnormal DNA methyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17026e6488c812e1122dd3705a6deb7b
https://pubmed.ncbi.nlm.nih.gov/1944474
https://pubmed.ncbi.nlm.nih.gov/1944474
