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The fragile X phenotype in a mosaic male with a deletion showing expression of theFMR1 protein in 28% of the cells
de Graaff, Esther, de Vries, Bert B. A., Willemsen, Rob, van Hemel, Jan O., Mohkamsing, Serieta, Oostra, Ben A., van den Ouweland, Ans M. W.Volume:
64
Language:
english
Pages:
7
Journal:
American Journal of Medical Genetics
DOI:
10.1002/(sici)1096-8628(19960809)64:23.0.co;2-j
Date:
August, 1996
File:
PDF, 790 KB
english, 1996