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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 1 |
2019 | 2 |
2020 | 1 |
2024 | 0 |
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Page 1
Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis.
Orphanet J Rare Dis. 2019 Aug 9;14(1):195. doi: 10.1186/s13023-019-1170-x.
Orphanet J Rare Dis. 2019.
PMID: 31399107
Free PMC article.
Review.
Perinatal diagnosis and management of early-onset Marfan syndrome: case report and systematic review.
Veiga-Fernández A, Joigneau Prieto L, Álvarez T, Ruiz Y, Pérez R, Gámez F, Ortega Abad V, Yllana F, De León-Luis J.
Veiga-Fernández A, et al.
J Matern Fetal Neonatal Med. 2020 Jul;33(14):2493-2504. doi: 10.1080/14767058.2018.1552935. Epub 2019 Jan 17.
J Matern Fetal Neonatal Med. 2020.
PMID: 30652519
In the postnatally diagnosed cases, the most frequent findings were arachnodactyly, dilatation of the great vessels and mitral or tricuspid regurgitation. ...
In the postnatally diagnosed cases, the most frequent findings were arachnodactyly, dilatation of the great vessels and mitral or tri …
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Non-pharmacological treatment of psychiatric disorders in individuals with 22q11.2 deletion syndrome; a systematic review.
Buijs PCM, Bassett AS, Boot E.
Buijs PCM, et al.
Am J Med Genet A. 2018 Aug;176(8):1742-1747. doi: 10.1002/ajmg.a.38612. Epub 2018 Jan 24.
Am J Med Genet A. 2018.
PMID: 29363845
Free PMC article.
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