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Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies.
Circ Cardiovasc Genet. 2015 Aug;8(4):572-581. doi: 10.1161/CIRCGENETICS.115.001086. Epub 2015 May 11.
Circ Cardiovasc Genet. 2015.
PMID: 25963545
Free PMC article.
Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study.
Balendra R, Uphill J, Collinson C, Druyeh R, Adamson G, Hummerich H, Zerr I, Gambetti P, Collinge J, Mead S.
Balendra R, et al.
BMC Med Genet. 2016 Apr 7;17:28. doi: 10.1186/s12881-016-0278-2.
BMC Med Genet. 2016.
PMID: 27055460
Free PMC article.
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Noninvasive Prenatal Diagnosis for Cystic Fibrosis: Implementation, Uptake, Outcome, and Implications.
Chandler NJ, Ahlfors H, Drury S, Mellis R, Hill M, McKay FJ, Collinson C, Hayward J, Jenkins L, Chitty LS.
Chandler NJ, et al.
Clin Chem. 2020 Jan 1;66(1):207-216. doi: 10.1373/clinchem.2019.305011.
Clin Chem. 2020.
PMID: 31551312
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