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R Rupps

Showing results (1-10 of 7) with videos related to

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Infection and Immunity|November 1, 1994
Cloning, sequencing, and viscometric adhesion analysis of heat-resistant agglutinin 1, an integral membrane hemagglutinin from Escherichia coli O9:H10:K99P Lutwyche, R Rupps, J Cavanagh, et al.
Alaska Medicine|October 13, 2007
Congenital heart defects in Canadian Inuit: is more folic acid making a difference?L Arbour, R Rupps, S MacDonald, et al.
American Journal of Medical Genetics|September 12, 2000
Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell lineH Bruyère, R Rupps, B D Kuchinka, et al.
Clinical Genetics|October 7, 2005
Recurrent trisomy 21: four cases in three generationsJ L Gair, L Arbour, R Rupps, et al.
American Journal of Medical Genetics|March 10, 2001
Renal-coloboma syndrome: prenatal detection and clinical spectrum in a large familyB Ford, R Rupps, D Lirenman, et al.
American Journal of Medical Genetics|August 23, 1996
Skeletal and cardiac malformations with thrombocytopenia: a new syndrome?R Rupps, A M Elliott, E M Azouz, et al.
Clinical Genetics|August 19, 2014
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorderA Chaudhry, A Noor, B Degagne, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Infection and Immunity|November 1, 1994
Cloning, sequencing, and viscometric adhesion analysis of heat-resistant agglutinin 1, an integral membrane hemagglutinin from Escherichia coli O9:H10:K99P Lutwyche, R Rupps, J Cavanagh, et al.
Alaska Medicine|October 13, 2007
Congenital heart defects in Canadian Inuit: is more folic acid making a difference?L Arbour, R Rupps, S MacDonald, et al.
American Journal of Medical Genetics|September 12, 2000
Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell lineH Bruyère, R Rupps, B D Kuchinka, et al.
Clinical Genetics|October 7, 2005
Recurrent trisomy 21: four cases in three generationsJ L Gair, L Arbour, R Rupps, et al.
American Journal of Medical Genetics|March 10, 2001
Renal-coloboma syndrome: prenatal detection and clinical spectrum in a large familyB Ford, R Rupps, D Lirenman, et al.
American Journal of Medical Genetics|August 23, 1996
Skeletal and cardiac malformations with thrombocytopenia: a new syndrome?R Rupps, A M Elliott, E M Azouz, et al.
Clinical Genetics|August 19, 2014
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorderA Chaudhry, A Noor, B Degagne, et al.
Pageof 1