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Conditional Survival in Uveal Melanoma.
Ophthalmol Retina. 2021 Jun;5(6):536-542. doi: 10.1016/j.oret.2020.09.015. Epub 2020 Sep 23.
Ophthalmol Retina. 2021.
PMID: 32979556
A novel nicastrin mutation in a three-generation Dutch family with hidradenitis suppurativa: a search for functional significance.
Vossen ARJV, van Straalen KR, Swagemakers SMA, de Klein JEMM, Stubbs AP, Venter DJ, van der Zee HH, van der Spek PJ, Prens EP.
Vossen ARJV, et al. Among authors: de klein jemm.
J Eur Acad Dermatol Venereol. 2020 Oct;34(10):2353-2361. doi: 10.1111/jdv.16310. Epub 2020 Mar 12.
J Eur Acad Dermatol Venereol. 2020.
PMID: 32078194
Free PMC article.
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X chromosome inactivation in a female carrier of a 1.28 Mb deletion encompassing the human X inactivation centre.
de Hoon B, Splinter E, Eussen B, Douben JCW, Rentmeester E, van de Heijning M, Laven JSE, de Klein JEMM, Liebelt J, Gribnau J.
de Hoon B, et al. Among authors: de klein jemm.
Philos Trans R Soc Lond B Biol Sci. 2017 Nov 5;372(1733):20160359. doi: 10.1098/rstb.2016.0359.
Philos Trans R Soc Lond B Biol Sci. 2017.
PMID: 28947658
Free PMC article.
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Early diagnosis of Wolf-Hirschhorn syndrome triggered by a life-threatening event: congenital diaphragmatic hernia.
van Dooren MF, Brooks AS, Hoogeboom AJ, van den Hoonaard TL, de Klein JE, Wouters CH, Tibboel D.
van Dooren MF, et al.
Am J Med Genet A. 2004 Jun 1;127A(2):194-6. doi: 10.1002/ajmg.a.20613.
Am J Med Genet A. 2004.
PMID: 15108210
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Whole exome sequencing of known eye genes reveals genetic causes for high myopia.
Haarman AEG, Thiadens AAHJ, van Tienhoven M, Loudon SE, de Klein JEMMA, Brosens E, Polling JR, van der Schoot V, Bouman A, Kievit AJA, Hoefsloot LH, Klaver CCW, Verhoeven VJM.
Haarman AEG, et al. Among authors: de klein jemma.
Hum Mol Genet. 2022 Sep 29;31(19):3290-3298. doi: 10.1093/hmg/ddac113.
Hum Mol Genet. 2022.
PMID: 35567543
Free PMC article.
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