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Surveillance of multiple congenital anomalies; searching for new associations.
Morris JK, Bergman JEH, Barisic I, Wellesley D, Tucker D, Limb E, Addor MC, Cavero-Carbonell C, Matias Dias C, Draper ES, Echevarría-González-de-Garibay LJ, Gatt M, Klungsøyr K, Lelong N, Luyt K, Materna-Kiryluk A, Nelen V, Neville A, Perthus I, Pierini A, Randrianaivo-Ranjatoelina H, Rankin J, Rissmann A, Rouget F, Sayers G, Wertelecki W, Kinsner-Ovaskainen A, Garne E. Morris JK, et al. Among authors: gatt m. Eur J Hum Genet. 2024 Apr;32(4):407-412. doi: 10.1038/s41431-023-01502-w. Epub 2023 Dec 5. Eur J Hum Genet. 2024. PMID: 38052905 Free PMC article. Review.
Prenatal diagnosis of severe structural congenital malformations in Europe.
Garne E, Loane M, Dolk H, De Vigan C, Scarano G, Tucker D, Stoll C, Gener B, Pierini A, Nelen V, Rösch C, Gillerot Y, Feijoo M, Tincheva R, Queisser-Luft A, Addor MC, Mosquera C, Gatt M, Barisic I. Garne E, et al. Among authors: gatt m. Ultrasound Obstet Gynecol. 2005 Jan;25(1):6-11. doi: 10.1002/uog.1784. Ultrasound Obstet Gynecol. 2005. PMID: 15619321 Free article.
Preventing neural tube defects in Europe: a missed opportunity.
Busby A, Abramsky L, Dolk H, Armstrong B, Addor MC, Anneren G, Armstrong N, Baguette A, Barisic I, Berghold A, Bianca S, Braz P, Calzolari E, Christiansen M, Cocchi G, Daltveit AK, De Walle H, Edwards G, Gatt M, Gener B, Gillerot Y, Gjergja R, Goujard J, Haeusler M, Latos-Bielenska A, McDonnell R, Neville A, Olars B, Portillo I, Ritvanen A, Robert-Gnansia E, Rösch C, Scarano G, Steinbicker V. Busby A, et al. Among authors: gatt m. Reprod Toxicol. 2005 Sep-Oct;20(3):393-402. doi: 10.1016/j.reprotox.2005.03.009. Reprod Toxicol. 2005. PMID: 15927445
Survey of informed consent for registration of congenital anomalies in Europe.
Busby A, Ritvanen A, Dolk H, Armstrong N, De Walle H, Riaño-Galán I, Gatt M, McDonnell R, Nelen V, Stone D. Busby A, et al. Among authors: gatt m. BMJ. 2005 Jul 16;331(7509):140-1. doi: 10.1136/bmj.331.7509.140. BMJ. 2005. PMID: 16020855 Free PMC article. No abstract available.
Maternal age-specific risk of non-chromosomal anomalies.
Loane M, Dolk H, Morris JK; EUROCAT Working Group. Loane M, et al. BJOG. 2009 Jul;116(8):1111-9. doi: 10.1111/j.1471-0528.2009.02227.x. Epub 2009 May 29. BJOG. 2009. PMID: 19485989 Free article.
301 results