Authors: Bruyere, H Rupps, R Kuchinka, BD Friedman, JM Robinson, WP

Citation: H. Bruyere et al., Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line, AM J MED G, 94(1), 2000, pp. 35-41

Authors: Penaherrera, MS Barrett, IJ Brown, CJ Langlois, S Yong, SL Lewis, S Bruyere, H Howard-Peebles, PN Kalousek, DK Robinson, WP

Citation: Ms. Penaherrera et al., An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta, CLIN GENET, 58(6), 2000, pp. 436-446

Authors: Bruyere, H Lewis, MES Wood, S MacLeod, P Langlois, S

Citation: H. Bruyere et al., Increasing evidence for a new X-linked mental retardation/epilepsy gene localized to Xp21.3-Xp22.1, AM J MED G, 86(4), 1999, pp. 401-401

Authors: Bruyere, H Lewis, S Wood, S MacLeod, PJ Langlois, S

Citation: H. Bruyere et al., Confirmation of linkage in X-linked infantile spasms (West syndrome) and refinement of the disease locus to Xp21.3-Xp22.1, CLIN GENET, 55(3), 1999, pp. 173-181