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Cell, ISSN 0092-8674, 04/2014, Volume 157, Issue 3, pp. 651 - 663
Journal Article
by Namavar, Yasmin and Barth, Peter G and Kasher, Paul R and van Ruissen, Fred and Brockmann, Knut and Bernert, Günther and Writzl, Karin and Ventura, Karen and Cheng, Edith Y and Ferriero, Donna M and Basel-Vanagaite, Lina and Eggens, Veerle R. C and Krägeloh-Mann, Ingeborg and de Meirleir, Linda and King, Mary and Graham, John M and von Moers, Arpad and Knoers, Nine and Sztriha, Laszlo and Korinthenberg, Rudolf and Dobyns, William B and Baas, Frank and Poll-The, Bwee Tien and van der Aa, Nathalie and Arts, Willem F. M and Ades, Lesley C and Bahi-Buisson, Nadia and Battini, Roberta and Bodamer, Olaf and Boltshauser, Eugen and Boycott, Kym and Brueton, Louise and Brussel, Wim and Chandler, K. E and Cowan, Frances M and Crow, Yanick and Debus, Otfried and Demir, Ercan and Hastanesi, Gazi and Eason, Jacqueline and Ferrie, Colin D and Fisher, Richard B and Foulds, Nicola and Freeman, Jeremy L and Gooskens, Rob and Haeussler, Martin and Hageman, Gerard and Hammersen, Gerhard and Horn, Denise and Isidor, Bertrand and van der Knaap, Marjo S and Kress, Wolfram and Kroisel, Peter M and Kyllerman, Mårten and Lachmeijer, A. M. A and Lunsing, Roelineke J and McGillivray, George and Möllmann, Susanne and Muntoni, Francesco and Nemeth, Anea H and Neufeld-Kaiser, Whitney and van Nieuwenhuizen, Onno and Ouvrier, Robert and Pálmafy, Beatrix and Peeters, E. A. J and Phillips, Joanna J and Price, Susan and Rankin, Julia and Régal, Luc and de Rijk-van Andel, J. F and Roelens, Filip and Rutledge, Joe C and Ryan, Monique M and Seidl, Rainer and Sellerer, Nina C and Shannon, Nora L and Sival, Deborah A and Snoeck, I. N and Straussberg, Rachel and Tijssen, Marina A. J and Verloo, Patrick and de Vries, L. S and Wargowski, David and Williams, Anew N and Windpassinger, Christian and PCH Consortium and Sahlgrenska akademin and Institute of Clinical Sciences, Section for the Health of Women and Children, Department of Pediatrics and Göteborgs universitet and Gothenburg University and Institutionen för kliniska vetenskaper, sektionen för kvinnors och barns hälsa, Avdelningen för pediatrik and Sahlgrenska Academy
Brain, ISSN 0006-8950, 2011, Volume 134, Issue Part 1, pp. 143 - 156
Journal Article
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 3, pp. 457 - 464
Journal Article
Orphanet journal of rare diseases, ISSN 1750-1172, 2014, Volume 9, Issue 1, pp. 23 - 23
Journal Article
Brain, ISSN 1460-2156, 01/2011, Volume 134, Issue Pt 1, pp. 143 - 56
Pontocerebellar hypoplasia is a group of autosomal recessive neurodegenerative disorders with prenatal onset. The common characteristics are cerebellar... 
Journal Article
Brain, ISSN 0006-8950, 01/2011, Volume 134, pp. 143 - 156
Pontocerebellar hypoplasia is a group of autosomal recessive neurodegenerative disorders with prenatal onset. The common characteristics are cerebellar... 
Journal Article
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