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Prenatal testing for uniparental disomy (UPD).
Jay AM, Roberts E, Davies T, Barnes I, Curtis M, Healey K, Davison EV. Jay AM, et al. Among authors: davison ev. Prenat Diagn. 2001 Jun;21(6):513. doi: 10.1002/pd.25. Prenat Diagn. 2001. PMID: 11438960 No abstract available.
Structural chromosome anomalies in congenital diaphragmatic hernia.
Howe DT, Kilby MD, Sirry H, Barker GM, Roberts E, Davison EV, Mchugo J, Whittle MJ. Howe DT, et al. Among authors: davison ev. Prenat Diagn. 1996 Nov;16(11):1003-9. doi: 10.1002/(SICI)1097-0223(199611)16:11<1003::AID-PD995>3.0.CO;2-D. Prenat Diagn. 1996. PMID: 8953633
Prader Willi syndrome with hypothyroidism.
Bhate MS, Robertson PE, Davison EV, Brummitt JA. Bhate MS, et al. Among authors: davison ev. J Ment Defic Res. 1989 Jun;33 ( Pt 3):235-44. doi: 10.1111/j.1365-2788.1989.tb01471.x. J Ment Defic Res. 1989. PMID: 2754723
40 results