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2001 | 1 |
2002 | 1 |
2024 | 0 |
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MECP2 mutations in Danish patients with Rett syndrome: high frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation pattern.
Eur J Hum Genet. 2001 Mar;9(3):178-84. doi: 10.1038/sj.ejhg.5200600.
Eur J Hum Genet. 2001.
PMID: 11313756
Spectrum of MECP2 mutations in Rett syndrome.
Bienvenu T, Villard L, De Roux N, Bourdon V, Fontes M, Beldjord C, Tardieu M, Jonveaux P, Chelly J; French Consortium for MECP2 Gene Analysis.
Bienvenu T, et al.
Genet Test. 2002 Spring;6(1):1-6. doi: 10.1089/109065702760093843.
Genet Test. 2002.
PMID: 12180070
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