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Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families.
Westerman AM, Entius MM, Boor PP, Koole R, de Baar E, Offerhaus GJ, Lubinski J, Lindhout D, Halley DJ, de Rooij FW, Wilson JH. Westerman AM, et al. Among authors: koole r. Hum Mutat. 1999;13(6):476-81. doi: 10.1002/(SICI)1098-1004(1999)13:6<476::AID-HUMU7>3.0.CO;2-2. Hum Mutat. 1999. PMID: 10408777
Peutz-Jeghers syndrome: 78-year follow-up of the original family.
Westerman AM, Entius MM, de Baar E, Boor PP, Koole R, van Velthuysen ML, Offerhaus GJ, Lindhout D, de Rooij FW, Wilson JH. Westerman AM, et al. Among authors: koole r. Lancet. 1999 Apr 10;353(9160):1211-5. doi: 10.1016/s0140-6736(98)08018-0. Lancet. 1999. PMID: 10217080
Digenic inheritance of mutations in the coproporphyrinogen oxidase and protoporphyrinogen oxidase genes in a unique type of porphyria.
van Tuyll van Serooskerken AM, de Rooij FW, Edixhoven A, Bladergroen RS, Baron JM, Joussen S, Merk HF, Steijlen PM, Poblete-Gutiérrez P, te Velde K, Wilson JH, Koole RH, van Geel M, Frank J. van Tuyll van Serooskerken AM, et al. J Invest Dermatol. 2011 Nov;131(11):2249-54. doi: 10.1038/jid.2011.186. Epub 2011 Jul 7. J Invest Dermatol. 2011. PMID: 21734717 Free article.
Retrospective analysis of clinical outcomes in bilateral cleft lip and palate patients after secondary alveolar bone grafting and premaxilla osteotomy, using a new dento-maxillary scoring system.
Bittermann GKP, van Es RJJ, de Ruiter AP, Bittermann AJN, Koole R, Rosenberg AJWP. Bittermann GKP, et al. Among authors: koole r. J Craniomaxillofac Surg. 2021 Feb;49(2):110-117. doi: 10.1016/j.jcms.2020.12.006. Epub 2020 Dec 15. J Craniomaxillofac Surg. 2021. PMID: 33357967 Free article.
175 results