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Results: 4

Authors: Oetting, William S. Mentink, Margaret M. Summers, C. Gail Lewis, Richard A. White, James G. King, Richard A.
Citation: S. Oetting, William et al., Three different frameshift mutations of the tyrosinase gene in type IA oculocutaneous albinism., American journal of human genetics , 49-I(1), 1991, pp. 199-206

Authors: Ricardi, Vincent M. Lewis, Richard A.
Citation: M. Ricardi, Vincent et A. Lewis, Richard, Penetrance of von recklinghausen neurofibromatosis: A distinction between predecessors and descendants, American journal of human genetics , 42(2), 1988, pp. 284-289

Authors: Merry, Diane E. Lesko, John G. Sosnoski, Donna M. Lewis, Richard A. Lubinsky, Mark Trask, Barbara van den Engh, Ger Collins, Francis S. Nussbaum, Robert L.
Citation: E. Merry, Diane et al., Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21, American journal of human genetics , 45-I(4), 1989, pp. 530-540

Authors: Heilstedt, Heidi A. Ballif, Blake C, Howard, Leslie A. Lewis, Richard A. Stal, Sauel Kashork, Catherine D. Bacino, Carlos A. Shapira, Stuart K. Shaffer, Lisa G.
Citation: A. Heilstedt, Heidi et al., Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the Syndrome, American journal of human genetics , 72(5), 2003, pp. 1200-1212
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