Authors: Rauen, KA Cotter, PD Bitts, SR Cox, VA Golabi, M

Citation: Ka. Rauen et al., Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: Identification of a candidate region for CFC syndrome, AM J MED G, 93(3), 2000, pp. 219-222

Authors: Ewart-Toland, A Yankowitz, J Winder, A Imagire, R Cox, VA Aylsworth, AS Golabi, M

Citation: A. Ewart-toland et al., Oculouriculovertebral abnormalities in children of diabetic mothers, AM J MED G, 90(4), 2000, pp. 303-309

Authors: Britt, KL Drummond, AE Cox, VA Dyson, M Wreford, NG Jones, MEE Simpson, ER Findlay, JK

Citation: Kl. Britt et al., An age-related ovarian phenotype in mice with targeted disruption of the Cyp 19 (aromatase) gene, ENDOCRINOL, 141(7), 2000, pp. 2614-2623

Authors: Enns, GM Roeder, E Chan, RT Catts, ZAK Cox, VA Golabi, M

Citation: Gm. Enns et al., Apparent cyclophosphamide (cytoxan) embryopathy: A distinct phenotype?, AM J MED G, 86(3), 1999, pp. 237-241

Authors: Enns, GM Cox, VA Golabi, M Immken, L Fisher, J Curry, C

Citation: Gm. Enns et al., Gastrointestinal tract anomalies in velocardiofacial syndrome, AM J MED G, 84(4), 1999, pp. 382-383

Authors: Ewart-Toland, A Enns, GM Cox, VA Mohan, GC Rosenthal, P Golabi, M

Citation: A. Ewart-toland et al., Severe congenital anomalies requiring transplantation in children with Kabuki syndrome, AM J MED G, 80(4), 1998, pp. 362-367