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Overcoming the barriers to the implementing computerized physician order entry systems in US hospitals: perspectives from senior management.
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.
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DEPINHO, RONALD A
One or more keywords matched the following items that are connected to
DEPINHO, RONALD A
Item Type
Name
Concept
Werner Syndrome
Academic Article
Telomere shortening exposes functions for the mouse Werner and Bloom syndrome genes.
Academic Article
Essential role of limiting telomeres in the pathogenesis of Werner syndrome.
Academic Article
Elevated telomere-telomere recombination in WRN-deficient, telomere dysfunctional cells promotes escape from senescence and engagement of the ALT pathway.
Concept
Werner Syndrome Helicase
Search Criteria
Werner Syndrome