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B Wirth

Showing results (1-10 of 119) with videos related to

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Human Mutation|February 19, 2000
An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA)B Wirth
Human Genetics|January 12, 2001
Exclusion of Htra2-beta1, an up-regulator of full-length SMN2 transcript, as a modifying gene for spinal muscular atrophyC Helmken, B Wirth
Journal of Insect Physiology|August 1, 1974
[Disk electrophoresis fractionation of hemolymph proteins during the metamorphosis of different castes and sexes of Formica pratensis]G Schmidt, B Wirth
Nucleic Acids Research|March 11, 1992
A new polymorphic probe on 5q11.2-13.3: ECB306Bg12.1 (D5S215)K Rüther, B Wirth
Nucleic Acids Research|April 25, 1989
XmnI polymorphism of the human STS geneB Wirth, A Gal
International Journal of Emergency Mental Health|February 24, 2001
The critical incident stress debriefing process for the Los Angeles County Fire Department: automatic and effectiveM Hokanson, B Wirth
Human Genetics|July 1, 1996
Frequent DNA variant in exon 2a of the survival motor neuron gene (SMN): a further possibility for distinguishing the two copies of the geneE T Hahnen, B Wirth
Psychosomatics|November 1, 1982
Thirst and weight gain during maintenance hemodialysisJ B Wirth, M F Folstein
American Journal of Human Genetics|December 1, 1994
Refining the map and defining flanking markers of the gene for autosomal recessive polycystic kidney disease on chromosome 6p21.1-p12G Mücher, B Wirth, K Zerres
The Journal of Physiology|January 1, 1978
The renin-angiotensin system and sodium appetiteJ T Fitzsimons, J B Wirth
Pageof 12

Showing results (1-10 of 119) with videos related to

Sort By:
Pageof 12
Human Mutation|February 19, 2000
An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA)B Wirth
Human Genetics|January 12, 2001
Exclusion of Htra2-beta1, an up-regulator of full-length SMN2 transcript, as a modifying gene for spinal muscular atrophyC Helmken, B Wirth
Journal of Insect Physiology|August 1, 1974
[Disk electrophoresis fractionation of hemolymph proteins during the metamorphosis of different castes and sexes of Formica pratensis]G Schmidt, B Wirth
Nucleic Acids Research|March 11, 1992
A new polymorphic probe on 5q11.2-13.3: ECB306Bg12.1 (D5S215)K Rüther, B Wirth
Nucleic Acids Research|April 25, 1989
XmnI polymorphism of the human STS geneB Wirth, A Gal
International Journal of Emergency Mental Health|February 24, 2001
The critical incident stress debriefing process for the Los Angeles County Fire Department: automatic and effectiveM Hokanson, B Wirth
Human Genetics|July 1, 1996
Frequent DNA variant in exon 2a of the survival motor neuron gene (SMN): a further possibility for distinguishing the two copies of the geneE T Hahnen, B Wirth
Psychosomatics|November 1, 1982
Thirst and weight gain during maintenance hemodialysisJ B Wirth, M F Folstein
American Journal of Human Genetics|December 1, 1994
Refining the map and defining flanking markers of the gene for autosomal recessive polycystic kidney disease on chromosome 6p21.1-p12G Mücher, B Wirth, K Zerres
The Journal of Physiology|January 1, 1978
The renin-angiotensin system and sodium appetiteJ T Fitzsimons, J B Wirth
Pageof 12