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