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Identification of NUP98 abnormalities in acute leukemia: JARID1A (12p13) as a new partner gene.
van Zutven LJ, Onen E, Velthuizen SC, van Drunen E, von Bergh AR, van den Heuvel-Eibrink MM, Veronese A, Mecucci C, Negrini M, de Greef GE, Beverloo HB. van Zutven LJ, et al. Among authors: van den heuvel eibrink mm, van drunen e. Genes Chromosomes Cancer. 2006 May;45(5):437-46. doi: 10.1002/gcc.20308. Genes Chromosomes Cancer. 2006. PMID: 16419055
A 600 kb triplication in the cat eye syndrome critical region causes anorectal, renal and preauricular anomalies in a three-generation family.
Knijnenburg J, van Bever Y, Hulsman LO, van Kempen CA, Bolman GM, van Loon RL, Beverloo HB, van Zutven LJ. Knijnenburg J, et al. Among authors: van zutven lj, van bever y, van kempen ca, van loon rl. Eur J Hum Genet. 2012 Sep;20(9):986-9. doi: 10.1038/ejhg.2012.43. Epub 2012 Mar 7. Eur J Hum Genet. 2012. PMID: 22395867 Free PMC article.
Phenotypic variability of atypical 22q11.2 deletions not including TBX1.
Verhagen JM, Diderich KE, Oudesluijs G, Mancini GM, Eggink AJ, Verkleij-Hagoort AC, Groenenberg IA, Willems PJ, du Plessis FA, de Man SA, Srebniak MI, van Opstal D, Hulsman LO, van Zutven LJ, Wessels MW. Verhagen JM, et al. Among authors: van zutven lj, van opstal d. Am J Med Genet A. 2012 Oct;158A(10):2412-20. doi: 10.1002/ajmg.a.35517. Epub 2012 Aug 14. Am J Med Genet A. 2012. PMID: 22893440
Social and medical need for whole genome high resolution NIPT.
Srebniak MI, Knapen MFCM, Govaerts LCP, Polak M, Joosten M, Diderich KEM, van Zutven LJCM, Prinsen KAKE, Riedijk S, Go ATJI, Galjaard RH, Hoefsloot LH, Van Opstal D. Srebniak MI, et al. Among authors: van zutven ljcm. Mol Genet Genomic Med. 2020 Jan;8(1):e1062. doi: 10.1002/mgg3.1062. Epub 2019 Dec 1. Mol Genet Genomic Med. 2020. PMID: 31790156 Free PMC article.
24 results