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Qualitative assessment of FMR1 (CGG)n triplet repeat status in normal, intermediate, premutation, full mutation, and mosaic carriers in both sexes: Implications for fragile X syndrome carrier and newborn screening (vol 12, pg 162, 2010)
被引:0
|作者:
Hantash, Feras M.
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中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
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页码:473 / 473
页数:1
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