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Citation: M. Al-saffar et al., Reply to letter to the editor by Willatt - "Partial trisomy of 2p and neuroblastoma", AM J MED G, 102(3), 2001, pp. 305-305

Authors: Sohocki, MM Perrault, I Leroy, BP Payne, AM Dharmaraj, S Bhattacharya, SS Kaplan, J Maumenee, IH Koenekoop, R Meire, FM Birch, DG Heckenlively, JR Daiger, SP

Citation: Mm. Sohocki et al., Prevalence of AIPL1 mutations in inherited retinal degenerative disease, MOL GEN MET, 70(2), 2000, pp. 142-150

Authors: Choremis, J Arlet, V Brown, K Bashour, M Young, M Dube, P Koenekoop, R

Citation: J. Choremis et al., Transient exotropia after posterior spinal fusion in a child: A new case, J AAPOS, 4(2), 2000, pp. 120-121

Authors: Al-Saffar, M Lemyre, E Koenekoop, R Duncan, AMV Der Kaloustian, VM

Citation: M. Al-saffar et al., Phenotype of a patient with pure partial trisomy 2p(p23 -> pter), AM J MED G, 94(5), 2000, pp. 428-432

Authors: Hine, TJ Pitchford, NJ Kingdom, FAA Koenekoop, R

Citation: Tj. Hine et al., Blindness and high suicide risk?, PSYCHOSOMAT, 41(4), 2000, pp. 370-371

Authors: Koenekoop, R Pina, AL Loyer, M Davidson, J Robitaille, J Maumenee, I Tombran-Tink, J

Citation: R. Koenekoop et al., Four polymorphic variations in the PEDF gene identified during the mutation screening of patients with Leber congenital amaurosis, MOL VIS, 5(10), 1999, pp. NIL_1-NIL_4