Localization of the Gene for Rapidly Progressive Autosomal Dominant Parkinsonism and Dementia with Pallido-Ponto-Nigral Degeneration to Chromosome 17q21
Wijker, Mario, Wszolek, Zbigniew K., Wolters, Eric C. H., Rooimans, Martin A., Pals, Gerard, Pfeiffer, Ronald F., Lynch, Timothy, Rodnitzky, R. L., Wilhelmsen, Kirk C., Arwert, Fré
Published in Human molecular genetics (01.01.1996)
Published in Human molecular genetics (01.01.1996)
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Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene
Wijker, M, Morgan, N V, Herterich, S, van Berkel, C G, Tipping, A J, Gross, H J, Gille, J J, Pals, G, Savino, M, Altay, C, Mohan, S, Dokal, I, Cavenagh, J, Marsh, J, van Weel, M, Ortega, J J, Schuler, D, Samochatova, E, Karwacki, M, Bekassy, A N, Abecasis, M, Ebell, W, Kwee, M L, de Ravel, T, CG Mathew
Published in European journal of human genetics : EJHG (01.01.1999)
Published in European journal of human genetics : EJHG (01.01.1999)
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Journal Article
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA
Foe, J R, Rooimans, M A, Bosnoyan-Collins, L, Alon, N, Wijker, M, Parker, L, Lightfoot, J, Carreau, M, Callen, D F, Savoia, A, Cheng, N C, van Berkel, C G, Strunk, M H, Gille, J J, Pals, G, Kruyt, F A, Pronk, J C, Arwert, F, Buchwald, M, Joenje, H
Published in Nature genetics (01.12.1996)
Published in Nature genetics (01.12.1996)
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Presynaptic nigrostriatal function in genetically tested asymptomatic relatives from the pallido-ponto-nigral degeneration family
Kishore, A, Wszolek, Z K, Snow, B J, de la Fuente-Fernandez, R, Arwert, F, Wijker, M, Schulzer, M, Calne, D B, Vingerhoets, F J
Published in Neurology (01.12.1996)
Published in Neurology (01.12.1996)
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Journal Article
Evidence for at Least Eight Fanconi Anemia Genes
Joenje, Hans, Oostra, Anneke B., Wijker, Mario, di Summa, Franca M., van Berkel, Carola G.M., Rooimans, Martin A., Ebell, Wolfram, van Weel, Margreet, Pronk, Jan C., Buchwald, Manuel, Arwert, Fré
Published in American journal of human genetics (01.10.1997)
Published in American journal of human genetics (01.10.1997)
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Journal Article
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA
Kruyt, Frank A.E, Buchwald, Manuel, Lightfoot, Jeff, Joenje, Hans, Strunk, Mark H.P, Cheng, Ngan C, Pronk, Jan C, Gille, Johan J.P, Pals, Gerard, Arwert, Fré, Alon, Noa, Savoia, Anna, Parker, Linda, Carreau, Madeleine, van Berkel, Carola G.M, Rooimans, Martin A, Wijker, Mario, Lo Ten Foe, Jerome R, Bosnoyan-Collins, Lucine, Callen, David F
Published in Nature genetics (01.11.1996)
Published in Nature genetics (01.11.1996)
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Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3
Jansen, Stander, Westerveld, Andries, Easton, Douglas F, Morgan, Neil V, Cohn, Richard J, de Ravel, Thomy J, Gibson, Rachel A, Joenje, Hans, Melchionda, Salvatore, Roberts, Irene, Pronk, Jan C, Arwert, Fré, Savoia, Anna, Mathew, Christopher G, Temtamy, Samia, Ford, Deborah, Wijker, Mario, Havenga, Charmaine, Ortega, Juan J
Published in Nature genetics (01.11.1995)
Published in Nature genetics (01.11.1995)
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The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region
WIJKER, M, LIGTENBERG, M. J. L, LUNGAROTTI, M. S, ARWERT, F, SCHOUTE, F, DEFESCHE, J. C, PALS, G, BOLHUIS, P. A, ROPERS, H. H, HULSEBOS, T. J. M, MENKO, F. H, VAN OOST, B. A
Published in American journal of human genetics (01.05.1995)
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Published in American journal of human genetics (01.05.1995)
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