A case of paternal uniparental disomy for chromosome 11

This publication has 15 references indexed in Scilit:

• Cytogenetic analysis of chorionic villi for prenatal diagnosis: An ACC collaborative study of U.K. data
  Prenatal Diagnosis, 1994
• Tetranucleotide repeat polymorphism at the D11S488 locus
  Human Molecular Genetics, 1993
• Uniparental disomy with normal phenotype
  The Lancet, 1992
• Cytogenetic results from the U.S. collaborative study on CVS
  Prenatal Diagnosis, 1992
• Chromosome 11 uniparental isodisomy predisposing to embryonal neoplasms
  The Lancet, 1991
• Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism
  Prenatal Diagnosis, 1991
• Uniparental paternal disomy in a genetic cancer-predisposing syndrome
  Nature, 1991
• Parental imprinting of the mouse H19 gene
  Nature, 1991
• The predictive value of cytogenetic diagnosis after CVS: 1500 cases
  Prenatal Diagnosis, 1990
• Chorionic villi sampling: cytogenetic and clinical findings in 500 pregnancies.
  BMJ, 1987