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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 1 |
2020 | 4 |
2024 | 0 |
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5 results
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Page 1
Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract.
J Clin Med. 2020 Mar 10;9(3):751. doi: 10.3390/jcm9030751.
J Clin Med. 2020.
PMID: 32164334
Free PMC article.
Renal Syndromic Hearing Loss Is Common in Childhood-onset Chronic Kidney Disease.
Kim JH, Lee DH, Lee B, Lim SH, Ahn YH, Kang HG, Ha IS, Cheong HI.
Kim JH, et al.
J Korean Med Sci. 2020 Nov 16;35(44):e364. doi: 10.3346/jkms.2020.35.e364.
J Korean Med Sci. 2020.
PMID: 33200591
Free PMC article.
Item in Clipboard
Genotype and Phenotype Analyses in Pediatric Patients with HNF1B Mutations.
Lim SH, Kim JH, Han KH, Ahn YH, Kang HG, Ha IS, Cheong HI.
Lim SH, et al.
J Clin Med. 2020 Jul 21;9(7):2320. doi: 10.3390/jcm9072320.
J Clin Med. 2020.
PMID: 32708349
Free PMC article.
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Features of Autosomal Recessive Alport Syndrome: A Systematic Review.
Lee JM, Nozu K, Choi DE, Kang HG, Ha IS, Cheong HI.
Lee JM, et al.
J Clin Med. 2019 Feb 3;8(2):178. doi: 10.3390/jcm8020178.
J Clin Med. 2019.
PMID: 30717457
Free PMC article.
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A Premature Baby with Severe Oligohydramnios and Hypotension: a Case Report of Renal Tubular Dysgenesis.
Min J, Cho MH, Bae SP, Shin SH, Ha IS, Cheong HI, Kang HG.
Min J, et al.
J Korean Med Sci. 2020 Aug 17;35(32):e283. doi: 10.3346/jkms.2020.35.e283.
J Korean Med Sci. 2020.
PMID: 32808512
Free PMC article.
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