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American Journal of Human Genetics|September 1, 1992
Linkage of Thomsen disease to the T-cell-receptor beta (TCRB) locus on chromosome 7q35J A Abdalla, W L Casley, H K Cousin, et al.
American Journal of Human Genetics|February 1, 1992
Cystic fibrosis in the Basque country: high frequency of mutation delta F508 in patients of Basque originT Casals, C Vázquez, C Lázaro, et al.
American Journal of Human Genetics|March 1, 1992
Genetic discrimination and the lawM R Natowicz, J K Alper, J S Alper
American Journal of Human Genetics|February 1, 1992
Factor IXMadrid 2: a deletion/insertion in factor IX gene which abolishes the sequence of the donor junction at the exon IV-intron d splice siteJ Solera, M Magallón, J Martin-Villar, et al.
American Journal of Human Genetics|January 1, 1992
Microdeletions of chromosome 17p13 as a cause of isolated lissencephalyS A Ledbetter, A Kuwano, W B Dobyns, et al.
American Journal of Human Genetics|January 1, 1992
Patterns of association between genetic variability in apolipoprotein (apo) B, apo AI-CIII-AIV, and cholesterol ester transfer protein gene regions and quantitative variation in lipid and lipoprotein traits: influence of gender and exogenous hormonesA Kessling, S Ouellette, O Bouffard, et al.
American Journal of Human Genetics|April 1, 1992
Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletionJ P Giacalone, U Francke
American Journal of Human Genetics|August 21, 2003
Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locusCatherine Bourgain, Sabine Hoffjan, Raluca Nicolae, et al.
American Journal of Human Genetics|March 1, 1992
Assignment of the urokinase-type plasminogen activator receptor gene (PLAUR) to chromosome 19q13.1-q13.2A D Børglum, A Byskov, P Ragno, et al.
American Journal of Human Genetics|July 1, 1992
Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locusL Spirio, B Otterud, D Stauffer, et al.
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