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Neurogenetics|April 28, 2009
A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?Esther Brusse, Danielle Majoor-Krakauer, Bianca M de Graaf, et al.
Human Molecular Genetics|July 11, 2000
The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteinsF Tamanini, L L Kirkpatrick, J Schonkeren, et al.
Human Genetics|October 1, 1993
Founder effect in a Belgian-Dutch fragile X populationS Buyle, E Reyniers, L Vits, et al.
The Biochemical Journal|December 1, 1990
Expression and routeing of human lysosomal alpha-glucosidase in transiently transfected mammalian cellsL H Hoefsloot, R Willemsen, M A Kroos, et al.
Molecular Psychiatry|August 9, 2006
Genetic and clinical analysis of a large Dutch Gilles de la Tourette familyA J M H Verkerk, D C Cath, H C van der Linde, et al.
Biochemical and Biophysical Research Communications|March 14, 2002
A double RING-H2 domain in RNF32, a gene expressed during sperm formationMarijke J van Baren, Herma C van der Linde, Guido J Breedveld, et al.
The European Respiratory Journal|October 3, 2009
Novel strategy to identify genetic risk factors for COPD severity: a genetic isolateC C van Diemen, D S Postma, Y S Aulchenko, et al.
Human Heredity|August 1, 2006
Heritability of serum iron, ferritin and transferrin saturation in a genetically isolated population, the Erasmus Rucphen Family (ERF) StudyO T Njajou, B Z Alizadeh, Y Aulchenko, et al.
Orphanet Journal of Rare Diseases|January 3, 2012
Congenital dyserythropoietic anemia type II: molecular analysis and expression of the SEC23B geneFrancesca Punzo, Aida M Bertoli-Avella, Saverio Scianguetta, et al.
Journal of Neuropathology and Experimental Neurology|May 10, 2013
FBXO7 immunoreactivity in α-synuclein-containing inclusions in Parkinson disease and multiple system atrophyTianna Zhao, Lies-Anne Severijnen, Marcel van der Weiden, et al.
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