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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2008 | 1 |
2019 | 1 |
2020 | 2 |
2024 | 0 |
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Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6.
Genet Med. 2020.
PMID: 31690835
Free PMC article.
Chromosome deletions in 13q33-34: report of four patients and review of the literature.
Walczak-Sztulpa J, Wisniewska M, Latos-Bielenska A, Linné M, Kelbova C, Belitz B, Pfeiffer L, Kalscheuer V, Erdogan F, Kuss AW, Ropers HH, Ullmann R, Tzschach A.
Walczak-Sztulpa J, et al.
Am J Med Genet A. 2008 Feb 1;146A(3):337-42. doi: 10.1002/ajmg.a.32127.
Am J Med Genet A. 2008.
PMID: 18203171
Review.
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Reduced anogenital distance, hematuria and left renal hypoplasia in a patient with 13q33.1-34 deletion: case report and literature review.
He X, Shen H, Fu H, Feng C, Liu Z, Jin Y, Mao J.
He X, et al.
BMC Pediatr. 2020 Jul 2;20(1):327. doi: 10.1186/s12887-020-02205-7.
BMC Pediatr. 2020.
PMID: 32616040
Free PMC article.
Review.
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