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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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome |
scientific article |
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A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome (English)
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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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