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Sally Martell

Showing results (11-20 of 13) with videos related to

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Orphanet Journal of Rare Diseases|August 10, 2011
Understanding the impact of 1q21.1 copy number variantChansonette Harvard, Emma Strong, Eloi Mercier, et al.
JCI Insight|October 5, 2016
Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysisHani Bagheri, Chansonette Badduke, Ying Qiao, et al.
Human Mutation|October 17, 2013
Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genesYing Qiao, Kajari Mondal, Valentina Trapani, et al.
Pageof 2

Showing results (11-20 of 13) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 13 results.
Orphanet Journal of Rare Diseases|August 10, 2011
Understanding the impact of 1q21.1 copy number variantChansonette Harvard, Emma Strong, Eloi Mercier, et al.
JCI Insight|October 5, 2016
Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysisHani Bagheri, Chansonette Badduke, Ying Qiao, et al.
Human Mutation|October 17, 2013
Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genesYing Qiao, Kajari Mondal, Valentina Trapani, et al.
Pageof 2