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1. Association of novel rare coding variants with juvenile idiopathic arthritis. Issue 5 (6th January 2021)

2. Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments. Issue 1 (December 2015)

3. Deep learning prediction of attention-deficit hyperactivity disorder in African Americans by copy number variation. Issue 21 (November 2021)

4. Descriptive evaluation of antibody responses to severe acute respiratory coronavirus virus 2 (SARS-CoV-2) infection in plasma and gingival crevicular fluid in a nursing home cohort—Arkansas, June–August 2020. (22nd November 2022)

5. Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments. Issue 1 (December 2016)

6. Genetic analysis for type 1 diabetes genes in juvenile dermatomyositis unveils genetic disease overlap. (16th February 2022)

9. Mitochondrial DNA Haplogroups and Susceptibility to Neuroblastoma. (25th February 2020)

10. Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing. Issue 22 (1st June 2022)