Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene (Q33677257)
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Current Data About Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene
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(P1476) "Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene" (language: en)
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(P2093) Milà M
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Castellví-Bel S
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Sánchez A
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Lázaro C
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Villa M
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External Links
(P356) 10.1136/JMG.33.4.338
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