Wijker M - Search Results

1

Presynaptic nigrostriatal function in genetically tested asymptomatic relatives from the pallido-ponto-nigral degeneration family.

Kishore A, Wszolek ZK, Snow BJ, de la Fuente-Fernandez R, Arwert F, Wijker M, Schulzer M, Calne DB, Vingerhoets FJ. Kishore A, et al. Among authors: wijker m. Neurology. 1996 Dec;47(6):1588-90. doi: 10.1212/wnl.47.6.1588. Neurology. 1996. PMID: 8960754

2

Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21.

Wijker M, Wszolek ZK, Wolters EC, Rooimans MA, Pals G, Pfeiffer RF, Lynch T, Rodnitzky RL, Wilhelmsen KC, Arwert F. Wijker M, et al. Hum Mol Genet. 1996 Jan;5(1):151-4. doi: 10.1093/hmg/5.1.151. Hum Mol Genet. 1996. PMID: 8789453

3

Evidence for at least eight Fanconi anemia genes.

Joenje H, Oostra AB, Wijker M, di Summa FM, van Berkel CG, Rooimans MA, Ebell W, van Weel M, Pronk JC, Buchwald M, Arwert F. Joenje H, et al. Among authors: wijker m. Am J Hum Genet. 1997 Oct;61(4):940-4. doi: 10.1086/514881. Am J Hum Genet. 1997. PMID: 9382107 Free PMC article.

4

Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.

Foe JR, Rooimans MA, Bosnoyan-Collins L, Alon N, Wijker M, Parker L, Lightfoot J, Carreau M, Callen DF, Savoia A, Cheng NC, van Berkel CG, Strunk MH, Gille JJ, Pals G, Kruyt FA, Pronk JC, Arwert F, Buchwald M, Joenje H. Foe JR, et al. Among authors: wijker m. Nat Genet. 1996 Dec;14(4):488. doi: 10.1038/ng1296-488. Nat Genet. 1996. PMID: 8944034 No abstract available.

5

Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.

Lo Ten Foe JR, Rooimans MA, Bosnoyan-Collins L, Alon N, Wijker M, Parker L, Lightfoot J, Carreau M, Callen DF, Savoia A, Cheng NC, van Berkel CG, Strunk MH, Gille JJ, Pals G, Kruyt FA, Pronk JC, Arwert F, Buchwald M, Joenje H. Lo Ten Foe JR, et al. Among authors: wijker m. Nat Genet. 1996 Nov;14(3):320-3. doi: 10.1038/ng1196-320. Nat Genet. 1996. PMID: 8896563

6

The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region.

Wijker M, Ligtenberg MJ, Schoute F, Defesche JC, Pals G, Bolhuis PA, Ropers HH, Hulsebos TJ, Menko FH, van Oost BA, et al. Wijker M, et al. Am J Hum Genet. 1995 May;56(5):1096-100. Am J Hum Genet. 1995. PMID: 7726164 Free PMC article.

7

Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.

Wijker M, Morgan NV, Herterich S, van Berkel CG, Tipping AJ, Gross HJ, Gille JJ, Pals G, Savino M, Altay C, Mohan S, Dokal I, Cavenagh J, Marsh J, van Weel M, Ortega JJ, Schuler D, Samochatova E, Karwacki M, Bekassy AN, Abecasis M, Ebell W, Kwee ML, de Ravel T, CG Mathew, et al. Wijker M, et al. Eur J Hum Genet. 1999 Jan;7(1):52-9. doi: 10.1038/sj.ejhg.5200248. Eur J Hum Genet. 1999. PMID: 10094191

8

Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3.

Pronk JC, Gibson RA, Savoia A, Wijker M, Morgan NV, Melchionda S, Ford D, Temtamy S, Ortega JJ, Jansen S, et al. Pronk JC, et al. Among authors: wijker m. Nat Genet. 1995 Nov;11(3):338-40. doi: 10.1038/ng1195-338. Nat Genet. 1995. PMID: 7581462

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