Associated Papers
Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders.
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Supplement: NIHMS64345-supplement-Supplementary_tables.xlsx › Table_S15
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Ryu GM et al.
Nucleic Acids Research, 2009
19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File009.xls › TypeI_
Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype.
Shrimpton AE et al.
Clinical Genetics, 2004
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