Publication | Closed Access
PGD in the lab for triplet repeat diseases ? myotonic dystrophy, Huntington's disease and Fragile-X syndrome
83
Citations
11
References
2001
Year
Triplet Repeat DiseasesMendelian DisorderGenetic DisorderMedicineGeneticsFragile X SpectrumNeurologyDisease Gene IdentificationNeurodegenerationNeuropathologyMyotonic DystrophyFragile-x SyndromeDevelopmental Delay
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