A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome (Q34332608)
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Current Data About A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome
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(P1476) "A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome" (language: en)
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(P2093) Meijer H
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de Graaff E
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Merckx DM
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Jongbloed RJ
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de Die-Smulders CE
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Engelen JJ
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Fryns JP
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Curfs PM
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Oostra BA
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External Links
(P356) 10.1093/HMG/3.4.615
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