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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 - 4 (of 4 Records)

Query Trace: Syndrome and NFATC1[original query]
From Genetic Predisposition to Molecular Mechanisms of Autoimmune Primary Adrenal Insufficiency.
Frontiers of hormone research 2016 46 115-32.
Falorni Alberto, Brozzetti Annalisa, Perniola Rober
CRELD1 gene variants and atrioventricular septal defects in Down syndrome.
Gene 2017 10 641 180-185.
Asim Ambreen, Agarwal Sarita, Panigrahi Inusha, Sarangi Aditya Narayan, Muthuswamy Srinivasan, Kapoor Adit
Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemia.
Blood 2020 11 137 (20): 2800-2816.
Klintman Jenny, Appleby Niamh, Stamatopoulos Basile, Ridout Katie, Eyre Toby A, Robbe Pauline, Pascua Laura Lopez, Knight Samantha J L, Dreau Helene, Cabes Maite, Popitsch Niko, Ehinger Mats, Martín-Subero Jose I, Campo Elías, Månsson Robert, Rossi Davide, Taylor Jenny C, Vavoulis Dimitrios V, Schuh An
Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans.
HGG advances 2022 Jan 3 (1): 100082.
Null Megan, Yilmaz Feyza, Astling David, Yu Hung-Chun, Cole Joanne B, Hallgrímsson Benedikt, Santorico Stephanie A, Spritz Richard A, Shaikh Tamim H, Hendricks Audrey
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