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Results: 1-4 |
Results: 4

Authors: Ikeda, Yoshio Dalton, Joline C. Moseley, Melinda L. Gardner, Kathy L. Bird, Thomas D. Ashizawa, Tetsuo Seltzer, William K. Pandolfo, Massimo Milunsky, Aubrey Potter, Nicholas T. Shoji, Mikio Vincent, John B. Day, John W. Ranum, Laura P.W.
Citation: Ikeda, Yoshio et al., Spinocerebellar Ataxia Type 8: Molecular Genetic Comparisonsand Haplotype Analysis of 37 Families with Ataxia, American journal of human genetics , 75(1), 2004, pp. 3-16

Authors: vanderSpek, Johanna C Wyandt, Herman E. Skare, James G. Milunsky, Aubrey Oppenheim, Frank G. Troxler, Robert F.
Citation: C. Vanderspek, Johanna et al., Localization of the genes for mistatins to human Chromosome 4q13 and tissue distribution of the mRNAs, American journal of human genetics , 45-I(3), 1989, pp. 381-387

Authors: Farrer, Lindsay A. Grundfast, Kenneth M Amos, Jean Arnos, Kathleen S. Asher, James H. Beighton, Peter Diehl, Scott R. Fex, Jörgen Foy, Carole Friedman, Thomas B. Greenberg, Jacquie Hoth, Christopher Marazita, Mary Milunsky, Aubrey Morell, Robert Nance, Walter Newton, Valerie Ramesar, Rajkumar San Agustin, Theresa B. Skare, James Stevens, Cathy A. Wagner, Ronald G. Wilcox,Edward R. Winship, Ingrid Read, Andrew P.
Citation: A. Farrer, Lindsay et al., Waardenberg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: First report of the WS consortium, American journal of human genetics , 50-II(5), 1992, pp. 902-913

Authors: Jones, Lee Anna Skare, James C. Harding, Jennifer A.. Cohen, AlanS. Milunsky, Aubrey Skinner, Martha
Citation: Jones, Lee Anna et al., Proline at position 36: a new transthyretin mutation associated with familial amyloidotic polyneuropathy., American journal of human genetics , 48-II(5), 1991, pp. 979-982
Risultati: 1-4 |