Early amniocentesis—a cytogenetic evaluation of over 1500 cases

This publication has 15 references indexed in Scilit:

• Fetal development after chorionic villus sampling
  The Lancet, 1993
• Prenatal diagnosis of monosomy 18 and ring chromosome 18 mosaicism
  Prenatal Diagnosis, 1992
• Importance of complete follow-up of spontaneous fetal loss after amniocentesis and chorion villus sampling
  The Lancet, 1992
• Introduction of early amniocentesis to routine prenatal diagnosis
  Prenatal Diagnosis, 1992
• Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies
  Prenatal Diagnosis, 1992
• First trimester amniocentesis between the seventh and 13th weeks: Evaluation of the earliest possible genetic diagnosis
  Prenatal Diagnosis, 1992
• Genetic amniocentesis at 7–14 weeks of gestation
  Prenatal Diagnosis, 1992
• Chang medium raises the chromatin instability of pericentromeric areas of chromosome 1 in amniotic fluid cells
  Prenatal Diagnosis, 1992
• Early amniocentesis at 11–14 weeks' gestation for the diagnosis of fetal chromosomal abnormality—a clinical evaluation
  Prenatal Diagnosis, 1991
• Prospective study of amniocentesis performed between weeks 9 and 16 of gestation: Its feasibility, risks, complications and use in early genetic prenatal diagnosis
  American Journal of Medical Genetics, 1990