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Psychopathology|November 27, 2009
Psychiatric profile in rubinstein-taybi syndrome. A review and case reportW M A Verhoeven, S Tuinier, H J H Kuijpers, et al.
Journal of Medical Genetics|October 23, 1998
The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomaliesH E Cunliffe, L A McNoe, T A Ward, et al.
European Journal of Human Genetics : EJHG|August 10, 2006
A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?Ilse Gutierrez-Roelens, Luc De Roy, Caroline Ovaert, et al.
Biochimica Et Biophysica Acta|December 1, 1977
Fractionation of membrane vesicles. II. A method for separation of membrane vesicles bearing different enzymes by free-flow electrophoresisG Brunner, H G Heidrich, J R Golecki, et al.
Iranian Biomedical Journal|May 4, 2017
Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration FamiliesMohammad Ghofrani, Mahin Yahyaei, Han G. Brunner, et al.
Anticancer Research|September 1, 1996
Inhibition of glycosylphosphatidylinositol (GPI) phospholipase D by suramin-like compoundsG Brunner, L Zalkow, E Burgess, et al.
American Journal of Medical Genetics|March 1, 1992
Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalisB A Semmekrot, A Haraldsson, C M Weemaes, et al.
The Journal of Pediatrics|December 10, 1999
Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expressionI van der Burgt, G Thoonen, N Roosenboom, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
A new web-based data mining tool for the identification of candidate genes for human genetic disordersMarc A van Driel, Koen Cuelenaere, Patrick P C W Kemmeren, et al.
Neurology|January 1, 1991
Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathyH G Brunner, F Spaans, H J Smeets, et al.
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