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American Journal of Human Genetics|April 29, 2008
Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesisJanna Nousbeck, Ronen Spiegel, Akemi Ishida-Yamamoto, et al.
American Journal of Human Genetics|April 29, 2008
Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAPAlexandra Zhernakova, Eleanora M Festen, Lude Franke, et al.
American Journal of Human Genetics|April 29, 2008
Genetic architecture of transcript-level variation in humansShiwei Duan, R Stephanie Huang, Wei Zhang, et al.
American Journal of Human Genetics|April 29, 2008
Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive proteinAlexander P Reiner, Mathew J Barber, Yongtao Guan, et al.
American Journal of Human Genetics|March 29, 2008
Walking the interactome for prioritization of candidate disease genesSebastian Köhler, Sebastian Bauer, Denise Horn, et al.
American Journal of Human Genetics|March 29, 2008
Antisense masking of an hnRNP A1/A2 intronic splicing silencer corrects SMN2 splicing in transgenic miceYimin Hua, Timothy A Vickers, Hazeem L Okunola, et al.
American Journal of Human Genetics|April 1, 2008
FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormalityJ A Fantes, E Boland, J Ramsay, et al.
American Journal of Human Genetics|April 1, 2008
Y-chromosomal diversity in Lebanon is structured by recent historical eventsPierre A Zalloua, Yali Xue, Jade Khalife, et al.
American Journal of Human Genetics|February 1, 1991
Demonstration of the genuine iso-12p character of the standard marker chromosome of testicular germ cell tumors and identification of further chromosome 12 aberrations by competitive in situ hybridizationR F Suijkerbuijk, A Y van de Veen, J van Echten, et al.
American Journal of Human Genetics|June 3, 2008
Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arraysSeyedmehdi Shojaee, Farzad Sina, Setareh Sadat Banihosseini, et al.
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