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Nature Genetics|March 30, 2002
Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesisPaul D Gottlieb, Stephanie A Pierce, Robert J Sims, et al.Nature Genetics|December 22, 2005
APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathyAnne Rovelet-Lecrux, Didier Hannequin, Gregory Raux, et al.Nature Genetics|December 22, 2005
Nras loss induces metastatic conversion of Rb1-deficient neuroendocrine thyroid tumorChiaki Takahashi, Bernardo Contreras, Tsuyoshi Iwanaga, et al.Nature Genetics|October 29, 2009
Multiple loci influence erythrocyte phenotypes in the CHARGE ConsortiumSanthi K Ganesh, Neil A Zakai, Frank J A van Rooij, et al.Nature Genetics|September 1, 1993
A gene for familial hemiplegic migraine maps to chromosome 19A Joutel, M G Bousser, V Biousse, et al.Nature Genetics|September 1, 1993
Molecular genetic basis of the human Rhesus blood group systemI Mouro, Y Colin, B Chérif-Zahar, et al.Nature Genetics|July 1, 1997
Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1L Li, I D Krantz, Y Deng, et al.Nature Genetics|July 1, 1997
A component of the transcriptional repressor MeCP1 shares a motif with DNA methyltransferase and HRX proteinsS H Cross, R R Meehan, X Nan, et al.Nature Genetics|July 1, 1997
Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3M Chesi, E Nardini, L A Brents, et al.Nature Genetics|July 1, 1997
Correlation between severity and SMN protein level in spinal muscular atrophyS Lefebvre, P Burlet, Q Liu, et al.Pageof 744