Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome. (Q52008919)
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scientific article published in March 1996
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome. |
scientific article published in March 1996 |
Statements
Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome. (English)
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Eichler EE
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Macpherson JN
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Murray A
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Jacobs PA
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Chakravarti A
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Nelson DL
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1 March 1996
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5
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3
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319-330
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Identifiers
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