AAAAAA
Results:
1-9
|
Results: 9
Authors:
Upadhyaya, Meena
Sarfarazi, Mansoor
Huson, Susan M.
Broadhead, Wendy
Fryer, Alan
Harper, Peter S.
Citation: Upadhyaya, Meena et al., Close flanking markers for neurofibromatosis type I (NFI), American journal of human genetics , 44(1), 1989, pp. 41-47
Authors:
Harley, Helen G.
Brook, David
Floyd, Jo
Rundle, Shelley A.
Crow, Steven
Walsh, Kate V.
Thibault, Marie-Christine
Harper, Peter S.
Shaw, Duncan J.
Citation: G. Harley, Helen et al., Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker., American journal of human genetics , 49-I(1), 1991, pp. 68-75
Authors:
Zonana, Jonathan
Clarke, Angus
Sarfarazi, Mansoor
Thomas, Nicholas S. T.
Roberts, Kim
Marymee, Kathi
Harper, Peter S.
Citation: Zonana, Jonathan et al., X-linked hypohidrotic ectodermal dysplasia: localization within the region XqII-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis, American journal of human genetics , 43-I(1), 1988, pp. 75-85
Authors:
Robbins, Carolyn
Theilmann, Jane
Youngman, Sandra
Haines, Jonathan
Altherr, Michael J.
Harper, Peter S.
Payne, Cynthia
Junker, Ann
Wasmuth, John
Hayden, Michael R.
Citation: Robbins, Carolyn et al., Evidence from family studies that the gene causing huntington disease is telomeric to D4S95 and D4S90, American journal of human genetics , 44(3), 1989, pp. 422-425
Authors:
Harper, Peter S.
Citation: S. Harper, Peter, Huntington disease and the abuse of genetics, American journal of human genetics , 50-I(3), 1992, pp. 460-464
Authors:
Consalez, G. Giacomo
Thomas, Nick S. T.
Stayton, Carol L.
Knight, Samantha J. L.
Johnson, Mae
Hopkins, Linton C.
Harper, Peter S.
Elsas, Louis J.
Warren, Stephen T.
Citation: Consalez, G. Giacomo et al., Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative study., American journal of human genetics , 48-I(3), 1991, pp. 468-480
Authors:
Krawczak, Michael
Bockel, Barbara
Sandkuijl, Lodewijk
Thies, Ulrike
Fenton, Ian
Harper, Peter S.
Citation: Krawczak, Michael et al., Covariate-dependent age-at-onset distributions for Huntington disease., American journal of human genetics , 49-II(4), 1991, pp. 735-745
Authors:
Bachinski, Linda L.
Udd, Bjarne
Meola, Giovanni
Sansone, Valeria
Bassez, Guillaume
Eymard, Bruno
Thronton, Charles A.
Moxley, Richard T.
Harper, Peter S.
Rogers, Mark T.
Jurkat-Rott, Karin
Lehmann-Horn, Frank
Wieser, Thomas
Gamez, Josep
Navarro, Carmen
Bottani, Armand
Kohler, Andre
Shriver, Mark D.
Sallinen, Riitta
Wessman, Maija
Zhang, Shanxiang
Wright, Fred A.
Krahe, Ralf
Citation: L. Bachinski, Linda et al., Confirmation of the Type 2 Myotonic Dystrophy (CCTG)n Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect, American journal of human genetics , 73(4), 2003, pp. 835-848
Authors:
Koch, Manuela C.
Grimm, Tiemo
Harley, Helen G.
Harper, Peter S.
Citation: C. Koch, Manuela et al., Genetic risks for children of women with myotonic dystrophy., American journal of human genetics , 48-II(6), 1991, pp. 1084-1091
Risultati:
1-9
|