A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome.
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A. Poustka | B. Korn | K. Davies | H. Rott | A. Manca | D. Kotzot | G. Barbi | D. Wöhrle | M. Hirst | A. Schmidt | Annemarie Poustka | Antonella Manca | Bernhard Korn | Gotthold Barbi | Rott Hd | Kay E. Davies | K. E. Davies