Authors: O'Connell, P. Leach, R. J. Ledbetter, D. H. Cawthon, R. M. Culver, M. Eldridge, I. R. Frej, A.-K. Holm, T. R. Wolff, E. Thayer, M. J. Schafer, A. J. Fountain, J. W. Wallace, M. R. Collins, F. S. Skolnick, M. H. Rich, D. C. Fournier, R. E. K. Baty, B. J. Carey, I. C. Leppert, M. F. Lathrop, G. M. Lalouel, J.-M. White, R.

Citation: P. O'Connell, et al., Fine structure DNA mapping studies of the chromosomal region harboring the genetic defect in neurofibromatosis type I, American journal of human genetics , 44(1), 1989, pp. 51-57

Authors: Ledbetter, D. H. Mascarello, J. T. Riccardi, V. M. Harper, V. D. Airhart, S. D. Strobel, R. J.

Citation: H. Ledbetter, D. et al., Chromosome 15 Abnormalities and the Prade-Willi Syndrome: A Follow-Up Report of 40 Cases, American journal of human genetics , 34(2), 1982, pp. 278-285

Authors: Luty, J. A. Guo, Z. Willard, H. F. Ledbetter, D. H. Ledbetter, S. Litt, M.

Citation: A. Luty, J. et al., Five polymorphic microsatellite VNTRs on the human X chromosome, American journal of human genetics , 46-II(4), 1990, pp. 776-783

Authors: Ledbetter, D. H. Dumars, K. W. Carpenter, R. J. Caskey, C. T.

Citation: H. Ledbetter, D. et al., Amniotic-Fluid-Cell-Culture Failure and Syringe Toxicity Revisited, American journal of human genetics , 34(5), 1982, pp. 823-825