Genomic Imprinting in Humans

This publication has 140 references indexed in Scilit:

• Role for DNA methylation in genomic imprinting
  Nature, 1993
• Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
  Nature, 1993
• Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
  Published by Elsevier ,1992
• Monoallelic expression of the human H19 gene
  Nature Genetics, 1992
• Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
  Cell, 1991
• Absence of expression of the FMR-1 gene in fragile X syndrome
  Cell, 1991
• Replication asynchrony between homologs 15q11.2: Cytogenetic evidence for genomic imprinting
  Human Genetics, 1991
• Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations
  Somatic Cell and Molecular Genetics, 1990
• Identification of a mammalian protein that binds specifically to DNA containing methylated CpGs
  Published by Elsevier ,1989
• Fragile X syndrome
  The Journal of Pediatrics, 1987