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American Journal of Human Genetics|March 22, 2008
SNP arrays in heterogeneous tissue: highly accurate collection of both germline and somatic genetic information from unpaired single tumor samplesGuillaume Assié, Thomas LaFramboise, Petra Platzer, et al.American Journal of Human Genetics|March 25, 2008
Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson diseaseCorinne Lautier, Stefano Goldwurm, Alexandra Dürr, et al.American Journal of Human Genetics|February 29, 2008
Robust score statistics for QTL linkage analysisSamsiddhi Bhattacharjee, Chia-Ling Kuo, Nandita Mukhopadhyay, et al.American Journal of Human Genetics|February 29, 2008
The fine-scale and complex architecture of human copy-number variationGeorge H Perry, Amir Ben-Dor, Anya Tsalenko, et al.American Journal of Human Genetics|February 18, 2014
Mechanism, prevalence, and more severe neuropathy phenotype of the Charcot-Marie-Tooth type 1A triplicationPengfei Liu, Violet Gelowani, Feng Zhang, et al.American Journal of Human Genetics|March 1, 1988
Analyses of linked beta-globin genes suggest that nondeletion forms of hereditary persistence of fetal hemoglobin are bona fide switching mutantsJ E Metherall, F P Gillespie, B G ForgetAmerican Journal of Human Genetics|April 1, 1988
The Malmö polymorphism of coagulation factor IX, an immunologic polymorphism due to dimorphism of residue 148 that is in linkage disequilibrium with two other F.IX polymorphismsJ B Graham, D B Lubahn, S T Lord, et al.American Journal of Human Genetics|May 8, 2008
Differential expression of PTEN-targeting microRNAs miR-19a and miR-21 in Cowden syndromeMarcus G Pezzolesi, Petra Platzer, Kristin A Waite, et al.American Journal of Human Genetics|October 4, 2016
Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy NumberKyle Thompson, Homa Majd, Cristina Dallabona, et al.American Journal of Human Genetics|July 1, 1988
Characterization of six partial deletions in the low-density-lipoprotein (LDL) receptor gene causing familial hypercholesterolemia (FH)S Langlois, J J Kastelein, M R HaydenPageof 979