de Klein A - Search Results

1

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: de klein a, de krijger rr. 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.

2

Breakpoint heterogeneity in t(10;11) translocation in AML-M4/M5 resulting in fusion of AF10 and MLL is resolved by fluorescent in situ hybridization analysis.

Beverloo HB, Le Coniat M, Wijsman J, Lillington DM, Bernard O, de Klein A, van Wering E, Welborn J, Young BD, Hagemeijer A, et al. Beverloo HB, et al. Among authors: de klein a. Cancer Res. 1995 Oct 1;55(19):4220-4. Cancer Res. 1995. PMID: 7671224

3

Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindreds.

Devilee P, Cornelis RS, Bootsma A, Bardoel A, van Vliet M, van Leeuwen I, Cleton FJ, de Klein A, Lindhout D, Vasen HF, et al. Devilee P, et al. Among authors: de klein a. Am J Hum Genet. 1993 Apr;52(4):730-5. Am J Hum Genet. 1993. PMID: 8096358 Free PMC article.

4

Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization.

Naus NC, van Drunen E, de Klein A, Luyten GP, Paridaens DA, Alers JC, Ksander BR, Beverloo HB, Slater RM. Naus NC, et al. Among authors: de klein a. Genes Chromosomes Cancer. 2001 Mar;30(3):267-73. Genes Chromosomes Cancer. 2001. PMID: 11170284

5

Detection of genetic prognostic markers in uveal melanoma biopsies using fluorescence in situ hybridization.

Naus NC, Verhoeven AC, van Drunen E, Slater R, Mooy CM, Paridaens DA, Luyten GP, de Klein A. Naus NC, et al. Among authors: de klein a. Clin Cancer Res. 2002 Feb;8(2):534-9. Clin Cancer Res. 2002. PMID: 11839674

6

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: de klein a. Clin Genet. 2004 May;65(5):396-9. doi: 10.1111/j.0009-9163.2004.00244.x. Clin Genet. 2004. PMID: 15099347

7

Postmortem findings and clinicopathological correlation in congenital diaphragmatic hernia.

van Dooren MF, Goemaere NN, de Klein A, Tibboel D, de Krijger RR. van Dooren MF, et al. Among authors: de klein a, de krijger rr. Pediatr Dev Pathol. 2004 Sep-Oct;7(5):459-67. doi: 10.1007/s10024-004-1118-2. Epub 2004 Oct 6. Pediatr Dev Pathol. 2004. PMID: 15547770

8

Clinical and genetic analysis of patients with Saethre-Chotzen syndrome.

de Heer IM, de Klein A, van den Ouweland AM, Vermeij-Keers C, Wouters CH, Vaandrager JM, Hovius SE, Hoogeboom JM. de Heer IM, et al. Among authors: de klein a. Plast Reconstr Surg. 2005 Jun;115(7):1894-902; discussion 1903-5. doi: 10.1097/01.prs.0000165278.72168.51. Plast Reconstr Surg. 2005. PMID: 15923834

9

Concurrent loss of chromosome arm 1p and chromosome 3 predicts a decreased disease-free survival in uveal melanoma patients.

Kilic E, Naus NC, van Gils W, Klaver CC, van Til ME, Verbiest MM, Stijnen T, Mooy CM, Paridaens D, Beverloo HB, Luyten GP, de Klein A. Kilic E, et al. Among authors: de klein a. Invest Ophthalmol Vis Sci. 2005 Jul;46(7):2253-7. doi: 10.1167/iovs.04-1460. Invest Ophthalmol Vis Sci. 2005. PMID: 15980208

10

Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.

Bonifati V, Rohé CF, Breedveld GJ, Fabrizio E, De Mari M, Tassorelli C, Tavella A, Marconi R, Nicholl DJ, Chien HF, Fincati E, Abbruzzese G, Marini P, De Gaetano A, Horstink MW, Maat-Kievit JA, Sampaio C, Antonini A, Stocchi F, Montagna P, Toni V, Guidi M, Dalla Libera A, Tinazzi M, De Pandis F, Fabbrini G, Goldwurm S, de Klein A, Barbosa E, Lopiano L, Martignoni E, Lamberti P, Vanacore N, Meco G, Oostra BA; Italian Parkinson Genetics Network. Bonifati V, et al. Among authors: de gaetano a, de mari m, de pandis f, de klein a. Neurology. 2005 Jul 12;65(1):87-95. doi: 10.1212/01.wnl.0000167546.39375.82. Neurology. 2005. PMID: 16009891

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