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Scandinavian Journal of Gastroenterology. Supplement|January 1, 1983
Effect of sucralfate on peptic ulcer recurrence: a controlled double-blind multicenter studyM Classen, H Bethge, G Brunner, et al.
European Journal of Human Genetics : EJHG|September 11, 2008
Compound heterozygosity for two MSH2 mutations suggests mild consequences of the initiation codon variant c.1A>G of MSH2Carolien M Kets, Nicoline Hoogerbrugge, Joannes H J M van Krieken, et al.
Human Genetics|December 1, 1988
The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGKH G Brunner, A van Bennekom, E M Lambermon, et al.
Genomics|October 1, 1989
A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19H G Brunner, H Smeets, H M Lambermon, et al.
Human Molecular Genetics|December 6, 2001
CRB1 has a cytoplasmic domain that is functionally conserved between human and DrosophilaA I den Hollander, K Johnson, Y J de Kok, et al.
American Journal of Medical Genetics|April 10, 1995
Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier reportB C Hamel, J M Draaisma, A J Pinckers, et al.
Clinical Genetics|November 3, 2017
Homozygous mutation in ELMO2 may cause Ramon syndromeC Mehawej, A Hoischen, R A Farah, et al.
Nucleic Acids Research|June 28, 2005
GeneSeeker: extraction and integration of human disease-related information from web-based genetic databasesM A van Driel, K Cuelenaere, P P C W Kemmeren, et al.
Clinical Genetics|February 25, 2009
Dominant versus recessive traits conveyed by allelic mutations - to what extent is nonsense-mediated decay involved?S Ben-Shachar, M Khajavi, M A Withers, et al.
Tissue Engineering|December 3, 2002
Release of bioactive transforming growth factor beta(3) from microtextured polymer surfaces in vitro and in vivoJ A T C Parker, G Brunner, X F Walboomers, et al.
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