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Missing: sa% 3DU %2522q% 253D% 2522 3A% 2Fpubmed. 2F27340178%
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Welcome to NCBI. The National Center for Biotechnology Information advances science and health by providing access to biomedical and genomic information. About ...
Missing: sa% 3DU %2522q% 253D% 2522 3A% 2Fpubmed. 2F27340178%
Individuals with 22q11.2 deletion syndrome (22q11.2DS) can present with a wide range of features that are highly variable, even within families.
Missing: 3DU %2522q% 253D% 2522 3A% 2Fpubmed. 2F27340178%
Search all biomedical databases provided by the National Center for Biotechnology Information (NCBI), an agency of the U.S. National Library of Medicine at ...
Missing: q= sa% 3DU %2522q% 253D% 2522 3A% 2Fpubmed. 2F27340178%
A portal to gene-specific content based on NCBI's RefSeq project, information from model organism databases, and links to other resources.<br />
Missing: q= sa% 3DU %2522q% 253D% 2522 3A% 2Fpubmed. 2F27340178%
Aug 3, 2022 · 2) is a rare disease of genetic origin, caused by the loss of the q11.2 region of chromosome 22. It affects one in 4000 live newborns, and among ...
Missing: sa% 3DU %2522q% 253D% 2522 3A% 2Fpubmed. 2F27340178%
The Nucleotide database is a collection of sequences from several sources, including GenBank, RefSeq, TPA and PDB. Genome, gene and transcript sequence data ...
Missing: q= sa% 3DU %2522q% 253D% 2522 3A% 2Fpubmed. 2F27340178%
In vitro binding assays using recombinant proteins identified Vif peptides and monoclonal antibodies that inhibit Vif-APOBEC3G binding and suggested involvement ...
Missing: q= sa% 3DU %2522q% 253D% 2522 https% 3A% 2F% 2Fpubmed. 2F27340178% 2F
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