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M Gerding

Showing results (1-10 of 58) with videos related to

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Animal Genetics|May 11, 2013
Spotted Weimaraner dog due to de novo KIT mutationW M Gerding, D A Akkad, J T Epplen
The Netherlands Journal of Medicine|June 30, 2012
Severe hepatitis with coagulopathy due to HSV-1 in an immunocompetent manL Wind, M van Herwaarden, F Sebens, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1977
Sulfhaemoglobin. Absorption spectrum, millimolar extinction coefficient at lambda = 620 nm, and interference with the determination of haemoglobin and of haemiglobincy anideP Dijkhuizen, A Buursma, A M Gerding, et al.
Journal of Animal Breeding and Genetics = Zeitschrift Fur Tierzuchtung Und Zuchtungsbiologie|March 10, 2011
Tracing the origin of 'blue Weimaraner' dogs by molecular geneticsW M Gerding, S Schreiber, G Dekomien, et al.
Molecular and Cellular Probes|May 25, 2015
Multiple paternity and sperm storage in captive Hermann's tortoises, Testudo hermanni boettgeri determined from amniotic fluid adhering to the eggshellC M Farke, K Olek, W M Gerding, et al.
Journal of Neurology|December 18, 2010
Late onset Alexander's disease presenting as cerebellar ataxia associated with a novel mutation in the GFAP geneStephan Schmidt, Mike P Wattjes, Wanda M Gerding, et al.
Canine Genetics and Epidemiology|September 25, 2015
Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogsDenis A Akkad, Wanda M Gerding, Robin B Gasser, et al.
Journal of Medical Virology|May 1, 1994
Class and subclass distribution of Hantavirus-specific serum antibodies at different times after the onset of nephropathia epidemicaJ Groen, M Gerding, J G Jordans, et al.
Journal of the Neurological Sciences|April 7, 2009
Severe demyelinating hypertrophic polyneuropathy caused by a de novo frameshift mutation within the intracellular domain of myelin protein zero (MPZ/P0)Jana Zschüntzsch, Payam Dibaj, Sara Pilgram, et al.
Muscle & Nerve|November 3, 2009
Unusual Charcot-Marie-Tooth phenotype due to a mutation within the intracellular domain of myelin protein zeroChristiane Schneider-Gold, Judith Kötting, Jörg T Epplen, et al.
Pageof 6

Showing results (1-10 of 58) with videos related to

Sort By:
Pageof 6
Animal Genetics|May 11, 2013
Spotted Weimaraner dog due to de novo KIT mutationW M Gerding, D A Akkad, J T Epplen
The Netherlands Journal of Medicine|June 30, 2012
Severe hepatitis with coagulopathy due to HSV-1 in an immunocompetent manL Wind, M van Herwaarden, F Sebens, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1977
Sulfhaemoglobin. Absorption spectrum, millimolar extinction coefficient at lambda = 620 nm, and interference with the determination of haemoglobin and of haemiglobincy anideP Dijkhuizen, A Buursma, A M Gerding, et al.
Journal of Animal Breeding and Genetics = Zeitschrift Fur Tierzuchtung Und Zuchtungsbiologie|March 10, 2011
Tracing the origin of 'blue Weimaraner' dogs by molecular geneticsW M Gerding, S Schreiber, G Dekomien, et al.
Molecular and Cellular Probes|May 25, 2015
Multiple paternity and sperm storage in captive Hermann's tortoises, Testudo hermanni boettgeri determined from amniotic fluid adhering to the eggshellC M Farke, K Olek, W M Gerding, et al.
Journal of Neurology|December 18, 2010
Late onset Alexander's disease presenting as cerebellar ataxia associated with a novel mutation in the GFAP geneStephan Schmidt, Mike P Wattjes, Wanda M Gerding, et al.
Canine Genetics and Epidemiology|September 25, 2015
Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogsDenis A Akkad, Wanda M Gerding, Robin B Gasser, et al.
Journal of Medical Virology|May 1, 1994
Class and subclass distribution of Hantavirus-specific serum antibodies at different times after the onset of nephropathia epidemicaJ Groen, M Gerding, J G Jordans, et al.
Journal of the Neurological Sciences|April 7, 2009
Severe demyelinating hypertrophic polyneuropathy caused by a de novo frameshift mutation within the intracellular domain of myelin protein zero (MPZ/P0)Jana Zschüntzsch, Payam Dibaj, Sara Pilgram, et al.
Muscle & Nerve|November 3, 2009
Unusual Charcot-Marie-Tooth phenotype due to a mutation within the intracellular domain of myelin protein zeroChristiane Schneider-Gold, Judith Kötting, Jörg T Epplen, et al.
Pageof 6