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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Syndrome and UFD1L[original query]
Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.
European journal of human genetics : EJHG 2012 Oct 20 (10): 1051-7.
Shashi Vandana, Francis Alan, Hooper Stephen R, Kranz Peter G, Zapadka Michael, Schoch Kelly, Ip Edward, Tandon Neeraj, Howard Timothy D, Keshavan Matcheri
Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome.
The Journal of biological chemistry 2015 Sep 290 (38): 23240-53.
Napoli Eleonora, Tassone Flora, Wong Sarah, Angkustsiri Kathleen, Simon Tony J, Song Gyu, Giulivi Cecil
Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis.
Frontiers in physiology 2017 8 612.
Giusti Betti, Sticchi Elena, De Cario Rosina, Magi Alberto, Nistri Stefano, Pepe Guglielmi
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