18p trisomy: A case of direct 18p duplication characterized by molecular cytogenetic analysis

This publication has 13 references indexed in Scilit:

• Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome
  European Journal of Human Genetics, 2004
• Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion
  Prenatal Diagnosis, 2003
• Prenatal ascertainment of an inherited dup(18p) associated with an apparently normal phenotype
  American Journal of Medical Genetics, 1991
• Partial trisomy 18 with minimal anomalies: Lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18
  American Journal of Medical Genetics, 1990
• Partial Trisomy of Chromosome 18 (pter→q12) following a Familial 18;21 Translocation rcp(18;21)(q12;q11)
  Human Heredity, 1989
• Sibs with tetrasomy 18p born to a mother with trisomy 18p.
  Journal of Medical Genetics, 1989
• Duplication 18p with mild influence on the phenotype
  American Journal of Medical Genetics, 1988
• Monosomy 18p and pure trisomy 18p in a family with translocation (7;18).
  Journal of Medical Genetics, 1983
• Partielle Trisomie 18 (Trisomie 18p) als Folge einer familiären balancierten Translokation t (14;18)
  Klinische Padiatrie, 1981
• Origin of a small metacentric chromosome: Familial and cytogenetic evidence
  Clinical Genetics, 1975