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Best practice no 178. Examination of the human placenta.
Hargitai B, Marton T, Cox PM. Hargitai B, et al. Among authors: cox pm. J Clin Pathol. 2004 Aug;57(8):785-92. doi: 10.1136/jcp.2003.014217. J Clin Pathol. 2004. PMID: 15280396 Free PMC article.
Pathological assessment of intrauterine growth restriction.
Cox P, Marton T. Cox P, et al. Best Pract Res Clin Obstet Gynaecol. 2009 Dec;23(6):751-64. doi: 10.1016/j.bpobgyn.2009.06.006. Epub 2009 Oct 23. Best Pract Res Clin Obstet Gynaecol. 2009. PMID: 19854107 Review.
Re: Stillbirth collection by Man et al.
Cox P, Marton T, Hargitai B, Coetzee A, Bowen C, Penman D, Evans M, Gannon C, French P, Cohen M, Holden S, Allotey J, Evans C, Murphy A, Turner K, Cullinane C, Stahlschmidt J, Kokai G, Al Adnani M, Marnerides A, Vadgama B, McPartland J. Cox P, et al. Ultrasound Obstet Gynecol. 2017 Feb;49(2):281-282. doi: 10.1002/uog.17380. Ultrasound Obstet Gynecol. 2017. PMID: 28169497 Free article. No abstract available.
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome.
Morgan NV, Brueton LA, Cox P, Greally MT, Tolmie J, Pasha S, Aligianis IA, van Bokhoven H, Marton T, Al-Gazali L, Morton JE, Oley C, Johnson CA, Trembath RC, Brunner HG, Maher ER. Morgan NV, et al. Am J Hum Genet. 2006 Aug;79(2):390-5. doi: 10.1086/506256. Epub 2006 Jun 20. Am J Hum Genet. 2006. PMID: 16826531 Free PMC article.
Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome).
Meyer E, Ricketts C, Morgan NV, Morris MR, Pasha S, Tee LJ, Rahman F, Bazin A, Bessières B, Déchelotte P, Yacoubi MT, Al-Adnani M, Marton T, Tannahill D, Trembath RC, Fallet-Bianco C, Cox P, Williams D, Maher ER. Meyer E, et al. Am J Hum Genet. 2010 Mar 12;86(3):471-8. doi: 10.1016/j.ajhg.2010.02.004. Epub 2010 Mar 4. Am J Hum Genet. 2010. PMID: 20206334 Free PMC article.
107 results