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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: Disease and DCLRE1C[original query]
Recurrent CYP2C19 deletion allele is associated with triple-negative breast cancer.
BMC cancer 2014 14 (1): 902.
Tervasmäki Anna, Winqvist Robert, Jukkola-Vuorinen Arja, Pylkäs Kat
Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families.
BMC cancer 2019 Apr 19 (1): 313.
Shahi Rajendra Bahadur, De Brakeleer Sylvia, Caljon Ben, Pauwels Ingrid, Bonduelle Maryse, Joris Sofie, Fontaine Christel, Vanhoeij Marian, Van Dooren Sonia, Teugels Erik, De Grève Jacqu
Polymorphisms of the DNA repair gene EXO1 modulate cognitive aging in old adults in a Taiwanese population.
DNA repair 2019 Mar 78 1-6.
Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yang Albert C, Tsai Shih-J
Case report: Artemis deficiency and 3M syndrome-coexistence of two distinct genetic disorders.
Frontiers in pediatrics 2023 7 11 1211254.
Ayca Ceylan, Ilyas Emre Tekdemir, Nadir Kocak, Ivan Kingyue Chinn, Jordan Scott Orange, Hasibe Art
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