JEWELL C. WARD, Ph.D., M.D., B.S.

Professor
Pediatrics-Genetics
 
Professor
WestTN Family Practice-Jackson

Office: 522 BOLING CENTER FOR DEVELOPMENTAL DISABILITIES
711 JEFFERSON AVENUE
MEMPHIS TN 381630000
Tel: (901) 287-6472
jward@uthsc.edu

Publications

  1. Pivnick, EK, Angle, B, Kaufman, RA, Hall, BD, Pitukcheewanont, P, Hersh, JH, Fowlkes, JL, Sanders, LP, O'Brien, JM, Carroll, GS, Gunther, WM, Morrow, HG, Burghen, GA, Ward, JC. Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: report of five new cases and review. Am J Med Genet, 90 (2), 131-40, 2000.
  2. Salim, MA, Alpert, BS, Ward, JC, Pyeritz, RE. Effect of beta-adrenergic blockade on aortic root rate of dilation in the Marfan syndrome. Am J Cardiol, 74 (6), 629-33, 1994.
  3. Raby, RB, Ward, JC, Herrod, HG. Propionic acidaemia and immunodeficiency. J Inherit Metab Dis, 17 (2), 250-1, 1994.
  4. Pivnick, EK, Burstein, S, Wilroy, RS, Kaufman, RA, Ward, JC. Hallermann-Streiff syndrome with hypopituitarism contributing to growth failure. Am J Med Genet, 41 (4), 503-7, 1991.
  5. Tharapel, AT, Qumsiyeh, MB, Martens, PR, Tharapel, SA, Dalton, JD, Ward, JC, Wilroy, RS. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes. Am J Med Genet, 40 (1), 117-20, 1991.
  6. Moore, CA, Ward, JC, Rivas, ML, Magill, HL, Whyte, MP. Infantile hypophosphatasia: autosomal recessive transmission to two related sibships. Am J Med Genet, 36 (1), 15-22, 1990.
  7. Ward, JC. Inborn errors of metabolism of acute onset in infancy. Pediatr Rev, 11 (7), 205-16, 1990.