Parental Origin–Dependent, Male Offspring–Specific Transmission-Ratio Distortion at Loci on the Human X Chromosome

This publication has 18 references indexed in Scilit:

• Mouse Choroideremia Gene Mutation Causes Photoreceptor Cell Degeneration and is not Transmitted through the Female Germline
  Human Molecular Genetics, 1997
• Non-Mendelian transmission at the Machado-Joseph disease locus in normal females: preferential transmission of alleles with smaller CAG repeats.
  Journal of Medical Genetics, 1997
• The Drosophila developmental gene fat facets has a human homologue in Xp11.4 which escapes X-inactivation and has related sequences on Yq11.2 [published erratum appears in Hum Mol Genet 1997 Feb;6(2):334-5]
  Human Molecular Genetics, 1996
• Non–mendelian inheritance of X chromosome markers in interspecific backcrosses
  Nature Genetics, 1996
• An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybrids
  Nature Genetics, 1996
• Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22
  Human Molecular Genetics, 1995
• A 2D crossover–based map of the human X chromosome as a model for map integration
  Nature Genetics, 1995
• Transmission‐ratio distortion of X chromosomes among male offspring of females with skewed X‐inactivation
  Developmental Genetics, 1995
• Escape from X inactivation in human and mouse
  Trends in Genetics, 1995
• Genetic linkage of cone–rod retinal dystrophy to chromosome 19q and evidence for segregation distortion
  Nature Genetics, 1994