Familial pericentric inversion (3)(p12q24)

This publication has 13 references indexed in Scilit:

• Pericentric inversions in man: personal experience and review of the literature
  Human Genetics, 1987
• Pericentric inversions in man. A French collaborative study. Groupe de Cytogénéticiens Français.
  1986
• Pericentric inversion inv(3)(p11q21).
  Journal of Medical Genetics, 1984
• Pericentric inversions
  Human Genetics, 1984
• Chromosome abnormalities in 150 couples with multiple spontaneous abortions
  Fertility and Sterility, 1982
• Variant chromosome 3 (inv3) in normal newborns and their parents, and in children with mental retardation
  Human Genetics, 1978
• Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).
  1975
• A cytogenetic survey of 14,069 newborn infants
  Clinical Genetics, 1975
• [Heterozygosity and homozygosity for a pericentric inversion of human chromosone 3].
  1974
• An inherited pericentric chromosomal inversion (46, inv3 [p-q+]) associated with skeletal anomalies
  The Journal of Pediatrics, 1971