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Christian Windpassinger

Showing results (1-10 of 69) with videos related to

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International Journal of Molecular Sciences|May 13, 2026
SAA4: An Underdog Within the Serum Amyloid a Superfamily?Ernst Malle, Corina Madreiter-Sokolowski, Christian Windpassinger
Gene|July 18, 2002
The human gamma-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expressionChristian Windpassinger, Peter M Kroisel, Klaus Wagner, et al.
BMC Medical Genetics|February 6, 2016
Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndromeMuzammil Ahmad Khan, Sumitra Mohan, Muhammad Zubair, et al.
Developmental Neurorehabilitation|December 6, 2013
General movements in genetic disorders: A first look into Cornelia de Lange syndromePeter B Marschik, Marina Soloveichick, Christian Windpassinger, et al.
BMC Medical Genetics|October 12, 2014
A novel single base pair duplication in WDR62 causes primary microcephalyVerena Rupp, Sobiah Rauf, Ishrat Naveed, et al.
Human Genetics|September 19, 2003
Refinement of the Silver syndrome locus on chromosome 11q12-q14 in four families and exclusion of eight candidate genesChristian Windpassinger, Klaus Wagner, Erwin Petek, et al.
AJP Reports|July 23, 2015
Surfactant Protein B Deficiency Caused by Homozygous C248X Mutation-A Case Report and Review of the LiteratureStefan Kurath-Koller, Bernhard Resch, Raimund Kraschl, et al.
Journal of Human Genetics|July 2, 2003
Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomaliesErwin Petek, Christian Windpassinger, Burkhard Simma, et al.
Annals of Human Genetics|November 22, 2016
The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future RecommendationsMuzammil Ahmad Khan, Saadullah Khan, Christian Windpassinger, et al.
Oncotarget|November 5, 2017
Histone deacetylase inhibitors vorinostat and panobinostat induce G1 cell cycle arrest and apoptosis in multidrug resistant sarcoma cell linesEva Bernhart, Nicole Stuendl, Heike Kaltenegger, et al.
Pageof 7

Showing results (1-10 of 69) with videos related to

Sort By:
Pageof 7
International Journal of Molecular Sciences|May 13, 2026
SAA4: An Underdog Within the Serum Amyloid a Superfamily?Ernst Malle, Corina Madreiter-Sokolowski, Christian Windpassinger
Gene|July 18, 2002
The human gamma-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expressionChristian Windpassinger, Peter M Kroisel, Klaus Wagner, et al.
BMC Medical Genetics|February 6, 2016
Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndromeMuzammil Ahmad Khan, Sumitra Mohan, Muhammad Zubair, et al.
Developmental Neurorehabilitation|December 6, 2013
General movements in genetic disorders: A first look into Cornelia de Lange syndromePeter B Marschik, Marina Soloveichick, Christian Windpassinger, et al.
BMC Medical Genetics|October 12, 2014
A novel single base pair duplication in WDR62 causes primary microcephalyVerena Rupp, Sobiah Rauf, Ishrat Naveed, et al.
Human Genetics|September 19, 2003
Refinement of the Silver syndrome locus on chromosome 11q12-q14 in four families and exclusion of eight candidate genesChristian Windpassinger, Klaus Wagner, Erwin Petek, et al.
AJP Reports|July 23, 2015
Surfactant Protein B Deficiency Caused by Homozygous C248X Mutation-A Case Report and Review of the LiteratureStefan Kurath-Koller, Bernhard Resch, Raimund Kraschl, et al.
Journal of Human Genetics|July 2, 2003
Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomaliesErwin Petek, Christian Windpassinger, Burkhard Simma, et al.
Annals of Human Genetics|November 22, 2016
The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future RecommendationsMuzammil Ahmad Khan, Saadullah Khan, Christian Windpassinger, et al.
Oncotarget|November 5, 2017
Histone deacetylase inhibitors vorinostat and panobinostat induce G1 cell cycle arrest and apoptosis in multidrug resistant sarcoma cell linesEva Bernhart, Nicole Stuendl, Heike Kaltenegger, et al.
Pageof 7