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G Brunner

Showing results (521-530 of 727) with videos related to

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Human Genetics|June 27, 2003
Novel types of mutation in the choroideremia ( CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exonJosé A J M van den Hurk, Dorien J R van de Pol, Bernd Wissinger, et al.
Biology of Reproduction|August 26, 2022
Ferumoxytol dynamic contrast enhanced magnetic resonance imaging identifies altered placental cotyledon perfusion in rhesus macaques†Daniel P Seiter, Sydney M Nguyen, Terry K Morgan, et al.
Plos Pathogens|October 27, 2017
Pegivirus avoids immune recognition but does not attenuate acute-phase disease in a macaque model of HIV infectionAdam L Bailey, Connor R Buechler, Daniel R Matson, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutationErsan Kalay, Abdullah Uzumcu, Elmar Krieger, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Genotype versus phenotype in families with androgen insensitivity syndromeA L Boehmer, O Brinkmann, H Brüggenwirth, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 1, 2021
Clinical impact of re-evaluating genes and variants implicated in dilated cardiomyopathySophie L V M Stroeks, Debby M E I Hellebrekers, Godelieve R F Claes, et al.
Human Mutation|July 22, 2010
Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasiaClaus E Ott, Gundula Leschik, Fabienne Trotier, et al.
European Journal of Human Genetics : EJHG|August 31, 2017
Propionic acidemia as a cause of adult-onset dilated cardiomyopathyMoniek Riemersma, Mark R Hazebroek, Appolonia T J M Helderman-van den Enden, et al.
Human Mutation|March 22, 2007
Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairmentRob W J Collin, Ersan Kalay, Jaap Oostrik, et al.
Clinical Genetics|October 21, 2021
The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 geneServi J C Stevens, Constance T R M Stumpel, Karin E M Diderich, et al.
Pageof 73

Showing results (521-530 of 727) with videos related to

Sort By:
Pageof 73
Human Genetics|June 27, 2003
Novel types of mutation in the choroideremia ( CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exonJosé A J M van den Hurk, Dorien J R van de Pol, Bernd Wissinger, et al.
Biology of Reproduction|August 26, 2022
Ferumoxytol dynamic contrast enhanced magnetic resonance imaging identifies altered placental cotyledon perfusion in rhesus macaques†Daniel P Seiter, Sydney M Nguyen, Terry K Morgan, et al.
Plos Pathogens|October 27, 2017
Pegivirus avoids immune recognition but does not attenuate acute-phase disease in a macaque model of HIV infectionAdam L Bailey, Connor R Buechler, Daniel R Matson, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutationErsan Kalay, Abdullah Uzumcu, Elmar Krieger, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Genotype versus phenotype in families with androgen insensitivity syndromeA L Boehmer, O Brinkmann, H Brüggenwirth, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 1, 2021
Clinical impact of re-evaluating genes and variants implicated in dilated cardiomyopathySophie L V M Stroeks, Debby M E I Hellebrekers, Godelieve R F Claes, et al.
Human Mutation|July 22, 2010
Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasiaClaus E Ott, Gundula Leschik, Fabienne Trotier, et al.
European Journal of Human Genetics : EJHG|August 31, 2017
Propionic acidemia as a cause of adult-onset dilated cardiomyopathyMoniek Riemersma, Mark R Hazebroek, Appolonia T J M Helderman-van den Enden, et al.
Human Mutation|March 22, 2007
Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairmentRob W J Collin, Ersan Kalay, Jaap Oostrik, et al.
Clinical Genetics|October 21, 2021
The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 geneServi J C Stevens, Constance T R M Stumpel, Karin E M Diderich, et al.
Pageof 73