Authors: Yu, HW Lee, MH Starck, L Elias, ER Irons, M Salen, G Patel, SB Tint, GS

Citation: Hw. Yu et al., Spectrum of Delta(7)-dehydrocholesterol reductase mutations in patients with the Smith-Lemli-Opitz (RSH) syndrome, HUM MOL GEN, 9(9), 2000, pp. 1385-1391

Authors: Yu, HW Lee, MH Starck, L Elias, ER Irons, M Salen, G Patel, SB Tint, GS

Citation: Hw. Yu et al., Spectrum of Delta 7-dehydrocholesterol reductase mutations in patients with the Smith-Lemli-Opitz (RSH) syndrome (vol 9, pg 1385, 2000), HUM MOL GEN, 9(12), 2000, pp. 1903-1903

Authors: Huang, TS Elias, ER Mulliken, JB Kirse, DJ Holmes, LB

Citation: Ts. Huang et al., A new syndrome: Heart defects, laryngeal anomalies, preaxial polydactyly, and colonic aganglionosis in sibs, GENET MED, 1(3), 1999, pp. 104-108

Authors: Wheeler, PG Sadeghi-Nejad, A Elias, ER

Citation: Pg. Wheeler et al., The 3C syndrome: Evolution of the phenotype and growth hormone deficiency, AM J MED G, 87(1), 1999, pp. 61-64

Authors: Metzl, JD Elias, ER Berul, CI

Citation: Jd. Metzl et al., An interesting case of infant sudden death: Severe hypertrophic cardiomyopathy in Pompe's disease, PACE, 22(5), 1999, pp. 821-822

Authors: Borer, JG Kaefer, M Barnewolt, CE Elias, ER Hobbs, N Retik, AB Peters, CA

Citation: Jg. Borer et al., Renal findings on radiological followup of patients with Beckwith-Wiedemann syndrome, J UROL, 161(1), 1999, pp. 235-239