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Citation: Yq. Wu et al., Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome, AM J HU GEN, 67(5), 2000, pp. 1327-1332

Authors: Berend, SA Horwitz, J McCaskill, C Shaffer, LG

Citation: Sa. Berend et al., Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes, AM J HU GEN, 66(6), 2000, pp. 1787-1793

Authors: Berend, SA Feldman, GL McCaskill, C Czarnecki, P Van Dyke, DL Shaffer, LG

Citation: Sa. Berend et al., Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy, AM J MED G, 82(3), 1999, pp. 275-281