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J Huizenga

Showing results (11-20 of 17) with videos related to

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Gene|August 26, 1998
Human PON2 gene at 7q21.3: cloning, multiple mRNA forms, and missense polymorphisms in the coding sequenceH Mochizuki, S W Scherer, T Xi, et al.
Physics in Medicine and Biology|August 13, 2008
A scintillating gas detector for 2D dose measurements in clinical carbon beamsE Seravalli, M de Boer, F Geurink, et al.
Physics in Medicine and Biology|November 6, 2012
Improved EMCCD gamma camera performance by SiPM pre-localizationS Salvador, M A N Korevaar, J W T Heemskerk, et al.
Genomics|February 1, 1996
Hereditary hemochromatosis: generation of a transcription map within a refined and extended map of the HLA class I regionA Totaro, J M Rommens, A Grifa, et al.
Genomics|September 1, 1996
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsL R Osborne, D Martindale, S W Scherer, et al.
Genes|February 25, 2023
Genotype and Phenotype Analyses of a Novel <i>WFS1</i> Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema, et al.
Nature Genetics|October 15, 1998
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsyB A Minassian, J R Lee, J A Herbrick, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Gene|August 26, 1998
Human PON2 gene at 7q21.3: cloning, multiple mRNA forms, and missense polymorphisms in the coding sequenceH Mochizuki, S W Scherer, T Xi, et al.
Physics in Medicine and Biology|August 13, 2008
A scintillating gas detector for 2D dose measurements in clinical carbon beamsE Seravalli, M de Boer, F Geurink, et al.
Physics in Medicine and Biology|November 6, 2012
Improved EMCCD gamma camera performance by SiPM pre-localizationS Salvador, M A N Korevaar, J W T Heemskerk, et al.
Genomics|February 1, 1996
Hereditary hemochromatosis: generation of a transcription map within a refined and extended map of the HLA class I regionA Totaro, J M Rommens, A Grifa, et al.
Genomics|September 1, 1996
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsL R Osborne, D Martindale, S W Scherer, et al.
Genes|February 25, 2023
Genotype and Phenotype Analyses of a Novel <i>WFS1</i> Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema, et al.
Nature Genetics|October 15, 1998
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsyB A Minassian, J R Lee, J A Herbrick, et al.
Pageof 2