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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 2 |
2021 | 1 |
2024 | 0 |
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Page 1
Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis.
Front Pediatr. 2019 Dec 17;7:506. doi: 10.3389/fped.2019.00506. eCollection 2019.
Front Pediatr. 2019.
PMID: 31921720
Free PMC article.
The relationship between endothelial progenitor cells and pulmonary arterial hypertension in children with congenital heart disease.
Sun HX, Li GJ, Du ZH, Bing Z, Ji ZX, Luo G, Pan SL.
Sun HX, et al.
BMC Pediatr. 2019 Dec 17;19(1):502. doi: 10.1186/s12887-019-1884-x.
BMC Pediatr. 2019.
PMID: 31847901
Free PMC article.
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Identification of a novel heterozygous SPTB mutation by whole genome sequencing in a Chinese patient with hereditary spherocytosis and atrial septal defect: a case report.
Du Z, Luo G, Wang K, Bing Z, Pan S.
Du Z, et al.
BMC Pediatr. 2021 Jun 28;21(1):291. doi: 10.1186/s12887-021-02771-4.
BMC Pediatr. 2021.
PMID: 34182956
Free PMC article.
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