Strong evidence that the common variant S384F in BRCA2 has no pathogenic relevance in hereditary breast cancer (Q24813671)
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English | Strong evidence that the common variant S384F in BRCA2 has no pathogenic relevance in hereditary breast cancer |
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Strong evidence that the common variant S384F in BRCA2 has no pathogenic relevance in hereditary breast cancer (English)
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Schmutzler RK
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Arnold N
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Wappenschmidt B
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Meindl A
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Fimmers R
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Rhiem K
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Brosig M
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Wardelmann E
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Mallmann P
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27 July 2005
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R775-9
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