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Journal of Dairy Science|March 18, 2014
Technical note: Evaluation of an ear-attached movement sensor to record cow feeding behavior and activityJ P Bikker, H van Laar, P Rump, et al.
Clinical Genetics|July 25, 2008
Drayer's syndrome of mental retardation, microcephaly, short stature and absent phalanges is caused by a recurrent deletion of chromosome 15(q26.2-->qter)P Rump, T Dijkhuizen, B Sikkema-Raddatz, et al.
Journal of Clinical Immunology|June 17, 2015
IL2RG reversion event in a common lymphoid progenitor leads to delayed diagnosis and milder phenotypeAmy P Hsu, Stefania Pittaluga, Bianca Martinez, et al.
Neurogenetics|October 22, 2005
A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effectP Rump, H H Lemmink, C C Verschuuren-Bemelmans, et al.
American Journal of Medical Genetics. Part A|January 18, 2006
Severe complications in a child with achondroplasia and two FGFR3 mutations on the same alleleP Rump, T G W Letteboer, J J P Gille, et al.
Neurogenetics|July 3, 2017
Male patients affected by mosaic PCDH19 mutations: five new casesI M de Lange, P Rump, R F Neuteboom, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|December 25, 2014
Common severe infections in chronic granulomatous diseaseBeatriz E Marciano, Christine Spalding, Alan Fitzgerald, et al.
Clinical Genetics|February 3, 2018
De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further reviewW M R van den Akker, I Brummelman, L M Martis, et al.
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