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History (9)
Rbfox2-coordinated alternative splicing of Mef2d and Rock2 controls myoblast fusion during myogenesis.
Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.
Ovarian stimulation for fertility preservation in women with cancer: A systematic review and meta-analysis comparing random and conventional starts.
Screening for mutations in a genetically heterogeneous disorder: DHPLC versus DNA sequence for mutation detection in multiple genes causing Charcot-Marie-Tooth neuropathy.
Replicative mechanisms for CNV formation are error prone.
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Replicative mechanisms for CNV formation are error prone.
Replicative mechanisms for CNV formation are error prone. Nat Genet. 2013 Nov; 45(11):1319-26.
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PubMed
subject areas
Base Sequence
DNA Breaks
DNA Copy Number Variations
DNA Repair
DNA Replication
Frameshift Mutation
Gene Rearrangement
Genetic Variation
Genotype
Humans
Sequence Analysis, DNA
Sequence Deletion
authors with profiles
JOHN BELMONT
JAMES LUPSKI
PHILIP HASTINGS
DAVUT PEHLIVAN