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Animal Genetics
|
May 11, 2013
Spotted Weimaraner dog due to de novo KIT mutation
W 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 man
L 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 anide
P 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 genetics
W 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 eggshell
C 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 gene
Stephan 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 dogs
Denis 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 epidemica
J 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 zero
Christiane Schneider-Gold, Judith Kötting, Jörg T Epplen, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 58) with videos related to
Sort By:
Page
of 6
Animal Genetics
|
May 11, 2013
Spotted Weimaraner dog due to de novo KIT mutation
W 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 man
L 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 anide
P 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 genetics
W 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 eggshell
C 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 gene
Stephan 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 dogs
Denis 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 epidemica
J 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 zero
Christiane Schneider-Gold, Judith Kötting, Jörg T Epplen, et al.
Page
of 6