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Year Number of Results
1991 1
1993 1
2000 1
2002 1
2004 1
2005 1
2006 2
2007 4
2009 1
2010 1
2024 0

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12 results

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Page 1
Phenotype-genotype correlation in a familial IGF1R microdeletion case.
Veenma DC, Eussen HJ, Govaerts LC, de Kort SW, Odink RJ, Wouters CH, Hokken-Koelega AC, de Klein A. Veenma DC, et al. Among authors: eussen hj. J Med Genet. 2010 Jul;47(7):492-8. doi: 10.1136/jmg.2009.070730. Epub 2009 Dec 2. J Med Genet. 2010. PMID: 19955558
Deletion of the TWIST gene in a large five-generation family.
De Heer IM, Hoogeboom AJ, Eussen HJ, Vaandrager JM, De Klein A. De Heer IM, et al. Among authors: eussen hj. Clin Genet. 2004 May;65(5):396-9. doi: 10.1111/j.0009-9163.2004.00244.x. Clin Genet. 2004. PMID: 15099347
Congenital diaphragmatic hernia associated with duplication of 11q23-qter.
Klaassens M, Scott DA, van Dooren M, Hochstenbach R, Eussen HJ, Cai WW, Galjaard RJ, Wouters C, Poot M, Laudy J, Lee B, Tibboel D, de Klein A. Klaassens M, et al. Among authors: eussen hj. Am J Med Genet A. 2006 Jul 15;140(14):1580-6. doi: 10.1002/ajmg.a.31321. Am J Med Genet A. 2006. PMID: 16770801 Free PMC article.
Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome.
van Hagen JM, van der Geest JN, van der Giessen RS, Lagers-van Haselen GC, Eussen HJ, Gille JJ, Govaerts LC, Wouters CH, de Coo IF, Hoogenraad CC, Koekkoek SK, Frens MA, van Camp N, van der Linden A, Jansweijer MC, Thorgeirsson SS, De Zeeuw CI. van Hagen JM, et al. Among authors: eussen hj. Neurobiol Dis. 2007 Apr;26(1):112-24. doi: 10.1016/j.nbd.2006.12.009. Epub 2006 Dec 20. Neurobiol Dis. 2007. PMID: 17270452
Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization.
Klaassens M, van Dooren M, Eussen HJ, Douben H, den Dekker AT, Lee C, Donahoe PK, Galjaard RJ, Goemaere N, de Krijger RR, Wouters C, Wauters J, Oostra BA, Tibboel D, de Klein A. Klaassens M, et al. Among authors: eussen hj. Am J Hum Genet. 2005 May;76(5):877-82. doi: 10.1086/429842. Epub 2005 Mar 4. Am J Hum Genet. 2005. PMID: 15750894 Free PMC article.
Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification.
Hes FJ, van der Luijt RB, Janssen AL, Zewald RA, de Jong GJ, Lenders JW, Links TP, Luyten GP, Sijmons RH, Eussen HJ, Halley DJ, Lips CJ, Pearson PL, van den Ouweland AM, Majoor-Krakauer DF. Hes FJ, et al. Among authors: eussen hj. Clin Genet. 2007 Aug;72(2):122-9. doi: 10.1111/j.1399-0004.2007.00827.x. Clin Genet. 2007. PMID: 17661816
12 results