Prenatal diagnosis of dichromatic 16p+ heteromorphisms in two unrelated families

This publication has 9 references indexed in Scilit:

• Myelodysplastic syndrome in a kindred with ins(16) (p11.2)
  Clinical Genetics, 2008
• An unusual variant chromosome 9 with an extra C-negative, G-dark segment in the short arm
  Clinical Genetics, 2008
• Euchromatic 16p + heteromorphism: First report in North America
  American Journal of Medical Genetics, 1990
• Duplication of euchromatin without phenotypic effects: A variant of chromosome 16
  American Journal of Medical Genetics, 1990
• Non C-banding variants in some normal families might be homogeneously staining regions
  Human Genetics, 1989
• An unusual variant of chromosome 16
  Human Genetics, 1988
• A new variant of chromosome 16
  Human Genetics, 1987
• A rare non-heterochromatic 9p+ variant in two amniotic fluid cell cultures
  Prenatal Diagnosis, 1984
• A G‐band study of chromosomes in liveborn infants
  Annals of Human Genetics, 1980