Cite
HARVARD Citation
Court, F. et al. (n.d.). Genome‐Wide Allelic Methylation Analysis Reveals Disease‐Specific Susceptibility to Multiple Methylation Defects in Imprinting Syndromes. Human mutation. 34 (4), pp. 595-602. [Online].
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Court, F. et al. (n.d.). Genome‐Wide Allelic Methylation Analysis Reveals Disease‐Specific Susceptibility to Multiple Methylation Defects in Imprinting Syndromes. Human mutation. 34 (4), pp. 595-602. [Online].