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Phenotype of COL3A1/COL5A2 deletion patients.
Eur J Med Genet. 2022 Oct;65(10):104593. doi: 10.1016/j.ejmg.2022.104593. Epub 2022 Aug 11.
Eur J Med Genet. 2022.
PMID: 35964930
Free article.
Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.
Srebniak MI, Boter M, Oudesluijs GO, Cohen-Overbeek T, Govaerts LC, Diderich KE, Oegema R, Knapen MF, van de Laar IM, Joosten M, Van Opstal D, Galjaard RJ.
Srebniak MI, et al. Among authors: van de laar im.
Mol Cytogenet. 2012 Mar 13;5(1):14. doi: 10.1186/1755-8166-5-14.
Mol Cytogenet. 2012.
PMID: 22413963
Free PMC article.
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