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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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2022 | 1 |
2023 | 3 |
2024 | 0 |
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Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research.
Genes (Basel). 2023 Jan 7;14(1):169. doi: 10.3390/genes14010169.
Genes (Basel). 2023.
PMID: 36672911
Free PMC article.
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions.
Blagowidow N, Nowakowska B, Schindewolf E, Grati FR, Putotto C, Breckpot J, Swillen A, Crowley TB, Loo JCY, Lairson LA, Óskarsdóttir S, Boot E, Garcia-Minaur S, Cristina Digilio M, Marino B, Coleman B, Moldenhauer JS, Bassett AS, McDonald-McGinn DM.
Blagowidow N, et al.
Genes (Basel). 2023 Jan 6;14(1):160. doi: 10.3390/genes14010160.
Genes (Basel). 2023.
PMID: 36672900
Free PMC article.
Review.
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Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression.
Campbell IM, Crowley TB, Jobaliya C, Bailey A, McGinn DE, Gaiser K, Bassett A, Gur RE, Morrow B, Emanuel BS, Franco AT, French D, Zackai EH, McDonald-McGinn DM, Lambert MP.
Campbell IM, et al.
Clin Genet. 2023 Jan;103(1):109-113. doi: 10.1111/cge.14227. Epub 2022 Sep 16.
Clin Genet. 2023.
PMID: 36075864
Free PMC article.
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