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A Case of “G 2 Deletion Syndrome”: Ring or Partial Monosomy? (46,XX,22r or 46,XX,22p- ?)
Published online by Cambridge University Press: 01 August 2014
Abstract
A case of “G 2 Deletion Syndrome” is reported, based on concordant cytogenetic, clinical and dermatoglyphic findings. The definition of the syndrome, as associated with either a ring or a partially deleted chromosome 22, is discussed. The resulting interpretation favours the hypothesis of deletion of the short arm extending into the centromere.
- Type
- Short Notes
- Information
- Acta geneticae medicae et gemellologiae: twin research , Volume 24 , Issue 3-4 , 07-10 1975 , pp. 311 - 313
- Copyright
- Copyright © The International Society for Twin Studies 1975