Associated Papers
Two novel heterozygous ADCY10 variants identified in Chinese pediatric patients with absorptive hypercalciuria: case report and literature review.
Ge Y et al.
Journal of Genetics, 2024
Use of whole-exome sequencing to identify a novel ADCY10 mutation in a patient with nephrolithiasis.
Wang C et al.
American Journal of Translational Research, 2020
Development and validation of a targeted next generation DNA sequencing panel outperforming whole exome sequencing for the identification of clinically relevant genetic variants.
Miller EM et al.
Oncotarget, 2017
29254223 (PubMed )
Supplement: oncotarget-08-102033-s003.xlsx › macrogen_wes.n65_t65.varscan.sn
Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan.
Ilyas M et al.
Bmc Genomics, 2015
25887915 (PubMed )
Supplement: 12864_2015_1290_MOESM7_ESM.xlsx › Sheet1
Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia.
Sheehan VA et al.
Plos One, 2014
A comprehensive gene mutation screen in men with asthenozoospermia.
Visser L et al.
Fertility and Sterility, 2011
Association of adenylate cyclase 10 (ADCY10) polymorphisms and bone mineral density in healthy adults.
Ichikawa S et al.
Calcified Tissue International, 2009
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