Comment on

• Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromes.

  Riegel M, Castellan C, Balmer D, Brecevic L, Schinzel A. Riegel M, et al. Am J Med Genet. 1999 Jan 29;82(3):249-53. doi: 10.1002/(sici)1096-8628(19990129)82:3<249::aid-ajmg10>3.0.co;2-8. Am J Med Genet. 1999. PMID: 10215549
• Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy.

  Berend SA, Feldman GL, McCaskill C, Czarnecki P, Van Dyke DL, Shaffer LG. Berend SA, et al. Am J Med Genet. 1999 Jan 29;82(3):275-81. doi: 10.1002/(sici)1096-8628(19990129)82:3<275::aid-ajmg15>3.0.co;2-2. Am J Med Genet. 1999. PMID: 10215554