A Rare Chromosomal Disorder – Isochromosome 18p Syndrome

Samankaltaisia teoksia

• Clinical relevance of cytogenetics to pediatric practice. Postnatal findings of Patau syndrome – Review of 5 cases
  Tekijä: PLAIASU, Vasilica, et al.
  Julkaistu: (2010)
• A rare case of de novo mosaicism: Deletion 18p and isochromosome 18q syndrome
  Tekijä: Udayakumar, Achandira M., et al.
  Julkaistu: (2013)
• Skeletal Dysplasia Presenting as a Neuromuscular Disorder – Report of a Family with Camurati-Engelmann Syndrome
  Tekijä: PLAIASU, Vasilica, et al.
  Julkaistu: (2015)
• Isochromosome X mosaicism in a child with Kabuki syndrome phenotype: A rare cytogenetic association
  Tekijä: Kumar, Jeevan M., et al.
  Julkaistu: (2011)
• The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.
  Tekijä: Callen, D F, et al.
  Julkaistu: (1990)