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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 CLCN5[original query]
Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations.
Pediatric nephrology (Berlin, Germany) 2009 Oct 24 (10): 1967-73.
Tosetto Enrica, Addis Maria, Caridi Gianluca, Meloni Cristiana, Emma Francesco, Vergine Gianluca, Stringini Gilda, Papalia Teresa, Barbano Giancarlo, Ghiggeri Gian Marco, Ruggeri Laura, Miglietti Nunzia, D Angelo Angela, Melis Maria Antonietta, Anglani Fran
A pharmacogenetic candidate gene study of tenofovir-associated Fanconi syndrome.
Pharmacogenetics and genomics 2015 Feb 25 (2): 82-92.
Dahlin Amber, Wittwer Matthias, de la Cruz Melanie, Woo Jonathan M, Bam Rujuta, Scharen-Guivel Valeska, Flaherty John, Ray Adrian S, Cihlar Tomas, Gupta Samir K, Giacomini Kathleen
Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.
Molecular genetics & genomic medicine 2019 8 7 (9): e883.
Yamamura Tomohiko, Nozu Kandai, Minamikawa Shogo, Horinouchi Tomoko, Sakakibara Nana, Nagano China, Aoto Yuya, Ishiko Shinya, Nakanishi Koichi, Shima Yuko, Nagase Hiroaki, Rossanti Rini, Ye Ming J, Nozu Yoshimi, Ishimori Shingo, Morisada Naoya, Kaito Hiroshi, Iijima Kazumo
Genetic testing enables a precision medicine approach for nephrolithiasis and nephrocalcinosis in pediatrics: a single-center cohort.
Molecular genetics and genomics : MGG 2022 May .
Huang Lin, Qi Chang, Zhu Gaohong, Ding Juanjuan, Yuan Li, Sun Jie, He Xuelian, Wang Xiaow
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