Citation: Kl. Taylor et Ae. Chudley, Meeting the needs of future physicians: a core curriculum initiative for postgraduate medical education at a Canadian university, MED EDUC, 35(10), 2001, pp. 973-982
Authors:
Innes, AM
Chudley, AE
Reed, MH
Shuckett, EP
Hildes-Ripstein, GE
Greenberg, CR
Citation: Am. Innes et al., Third case of cerebral, ocular, dental, auricular, skeletal anomalies (CODAS) syndrome, further delineating a new malformation syndrome: First reportof an affected male and review of literature, AM J MED G, 102(1), 2001, pp. 44-47
Citation: K. Galenzoski et Ae. Chudley, Genetic landmarks through philately: the Human Genome Project and the new millennium, CLIN GENET, 59(6), 2001, pp. 393-396
Authors:
Mhanni, AA
Chodirker, BN
Evans, JA
Menticouglou, S
Wiseman, N
MacDonald, N
Chudley, AE
Citation: Aa. Mhanni et al., Fetal hepatic haemangioendothelioma: a new association with elevated maternal serum alpha-fetoprotein, PRENAT DIAG, 20(5), 2000, pp. 433-435
Citation: Ae. Chudley, Genetic landmarks through philately - Jean Martin Charcot (1825-1893) and Charcot-Marie-Tooth disease, CLIN GENET, 57(6), 2000, pp. 420-422
Authors:
Prasad, C
Prasad, AN
Chodirker, BN
Lee, C
Dawson, AK
Jocelyn, LJ
Chudley, AE
Citation: C. Prasad et al., Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype, CLIN GENET, 57(2), 2000, pp. 103-109
Citation: Ae. Chudley, Genetic landmarks through philately - Crick, Watson and Wilkins: the scientists behind DNA structure, CLIN GENET, 57(1), 2000, pp. 26-28
Authors:
Chudley, AE
Tackels, DC
Lubs, HA
Arena, JF
Stoeber, WP
Kovnats, S
Stevenson, RE
Schwartz, CE
Citation: Ae. Chudley et al., X-linked mental retardation syndrome with seizures, hypogammaglobulinemia,and progressive gait disturbance is regionally mapped between Xq21.33 and Xq23, AM J MED G, 85(3), 1999, pp. 255-262
Citation: Am. Innes et Ae. Chudley, Genetic landmarks through philately - Henry Louis 'Lou' Gehrig and amyotrophic lateral sclerosis, CLIN GENET, 56(6), 1999, pp. 425-427