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
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