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Nederlands Tijdschrift Voor Geneeskunde|July 13, 2010
[A neonate with a congenital hand defect]Petra J G Zwijnenburg, J M Annet van HagenAmerican Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 15, 2010
Identical but not the same: the value of discordant monozygotic twins in genetic researchPetra J G Zwijnenburg, Hanne Meijers-Heijboer, Dorret I BoomsmaMolecular Psychiatry|February 6, 2024
A de novo missense mutation in synaptotagmin-1 associated with neurodevelopmental disorder desynchronizes neurotransmitter releaseMaaike A van Boven, Marta Mestroni, Petra J G Zwijnenburg, et al.American Journal of Medical Genetics. Part A|July 29, 2021
5q11.2 deletion syndrome revisited-Further narrowing of the smallest region of overlap for the main clinical characteristics of the syndromeAllan Bayat, Michael Bayat, Chantal Broers, et al.Journal of Immunology (Baltimore, Md. : 1950)|April 23, 2003
IL-1 receptor type 1 gene-deficient mice demonstrate an impaired host defense against pneumococcal meningitisPetra J G Zwijnenburg, Tom van der Poll, Sandrine Florquin, et al.Infection and Immunity|March 26, 2003
Interleukin-10 negatively regulates local cytokine and chemokine production but does not influence antibacterial host defense during murine pneumococcal meningitisPetra J G Zwijnenburg, Tom van der Poll, Sandrine Florquin, et al.Journal of Neuroimmunology|December 4, 2003
Chemotactic activity of CXCL5 in cerebrospinal fluid of children with bacterial meningitisPetra J G Zwijnenburg, Henrica M A de Bie, John J Roord, et al.Journal of Neuroimmunology|May 14, 2003
Interleukin-18 gene-deficient mice show enhanced defense and reduced inflammation during pneumococcal meningitisPetra J G Zwijnenburg, Tom van der Poll, Sandrine Florquin, et al.European Journal of Medical Genetics|October 5, 2014
First steps in exploring prospective exome sequencing of consanguineous couplesMarieke Teeuw, Quinten Waisfisz, Petra J G Zwijnenburg, et al.European Journal of Human Genetics : EJHG|April 5, 2012
Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritanceSahar Mansour, Marielle Swinkels, Paulien A Terhal, et al.Pageof 3