Dr. David Bick, MD – Huntsville, AL
Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States
Miller, M.J., Burrage, L.C., Gibson, J.B., Strenk, M.E., Lose, E.J., Bick, D.P., Elsea, S.H., Sutton, V.R., Sun, Q., Graham, B.H., Craigen, W.J., Zhang, V.W., Wong, L.C., Molecular Genetics and Metabolism, 1/1/2015Whole exome analysis identifies dominant COL4A1 mutations in patients with complex ocular phenotypes involving microphthalmia
Deml, B., Reis, L., Maheshwarti, M., Griffis, C., BICK, D., Semina, E., Clin Genet, 1/1/2014Ehtical issues in DNA sequencing in the neonate
Dimmock, D.P., Bick, D.P., Clin Perinatol, 1/1/2014
