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Keyword [ICF syndrome]
Result: 1 - 6 | Page: 1 of 1
1.
Mutations In DNA Methyltransferase DNMT3B In ICF Syndrome Affect Its Regulation By DNMT3L
2.
Epigenetics of tandem DNA repeats in FSH muscular dystrophy, the DNMT3B-deficient ICF syndrome, and ovarian epithelial tumors
3.
DNA methylation and constitutive heterochromatin in the ICF syndrome, FSHD syndrome, and normal human embryonic cell cultures
4.
Nucleolin binds specifically to methylated classical satellite DNA, the affected region in the rare genetic disorder ICF syndrome
5.
DNA hypomethylation and chromosomal rearrangements in the ICF syndrome and in cancer
6.
Functions Of ZBTB24 In Human T Lymphocytes
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