Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies

This publication has 30 references indexed in Scilit:

• Tissue- and Developmental Stage-Specific Imprinting of the Mouse Proinsulin Gene, Ins2
  Developmental Biology, 1995
• Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
  Nature Genetics, 1994
• Parental imprinting of autosomal mammalian genes
  Current Opinion in Genetics & Development, 1994
• Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting
  Nature Genetics, 1994
• Mosaic and polymorphic imprinting of the WT1 gene in humans
  Nature Genetics, 1994
• Maternal imprinting of human SNRPN, a gene deleted in Prader–Willi syndrome
  Nature Genetics, 1994
• Functional imprinting and epigenetic modification of the human SNRPN gene
  Human Molecular Genetics, 1993
• Allele-specific replication timing of imprinted gene regions
  Nature, 1993
• A microsatellite-based index map of human chromosome 11
  Human Molecular Genetics, 1993
• A genetic linkage map of the human genome
  Cell, 1987