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Deletion screening by fluorescence in situ hybridization in Rett syndrome patients.
Ann Genet. 2001 Oct-Dec;44(4):191-4. doi: 10.1016/s0003-3995(01)01088-7.
Ann Genet. 2001.
PMID: 11755104
MECP2 mutations or polymorphisms in mentally retarded boys: diagnostic implications.
Bourdon V, Philippe C, Martin D, Verloès A, Grandemenge A, Jonveaux P.
Bourdon V, et al. Among authors: grandemenge a.
Mol Diagn. 2003;7(1):3-7. doi: 10.1007/BF03260014.
Mol Diagn. 2003.
PMID: 14529314
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