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Markus Stumm

Showing results (1-10 of 26) with videos related to

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Expert Opinion on Medical Diagnostics|March 19, 2013
Fluorescence in situ hybridization techniques in medical diagnosticsMarkus Stumm, Holger Tönnies
Geburtshilfe Und Frauenheilkunde|September 4, 2025
Opportunities and Limitations of Modern High Throughput Sequencing in Invasive Prenatal DiagnosticsHeinz Gabriel, Markus Stumm
American Journal of Medical Genetics. Part A|April 1, 2004
Slow progression of ataxia-telangiectasia with double missense and in frame splice mutationsThilo Dörk, Regina Bendix-Waltes, Rolf-Dieter Wegner, et al.
Prenatal Diagnosis|April 21, 2012
'Normal' nuchal translucency: a justification to refrain from detailed scan? Analysis of 6858 cases with special reference to ethical aspectsRolf Becker, Lothar Schmitz, Stefania Kilavuz, et al.
Prenatal Diagnosis|February 20, 2004
Retrospective diagnosis and subsequent prenatal diagnosis of Nijmegen breakage syndromePetra Muschke, Hannswerner Gola, Raymonda Varon, et al.
The Prostate|March 3, 2004
Gain of androgen receptor gene copies in primary prostate cancer due to X chromosome polysomyAlbrecht Röpke, Andreas Erbersdobler, Peter Hammerer, et al.
Biomedicines|May 28, 2022
The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different ChromosomesAndré Weber, Thomas Liehr, Ahmed Al-Rikabi, et al.
Genes, Chromosomes & Cancer|July 18, 2006
High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11)Ilse Wieland, Petra Muschke, Marianne Volleth, et al.
European Journal of Pediatrics|November 9, 2006
Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTCSibylle Jakubiczka, Thomas Bettecken, Klaus Mohnike, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Genotype/phenotype analysis in a patient with pure and complete trisomy 12pWalter Zumkeller, Marianne Volleth, Petra Muschke, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Expert Opinion on Medical Diagnostics|March 19, 2013
Fluorescence in situ hybridization techniques in medical diagnosticsMarkus Stumm, Holger Tönnies
Geburtshilfe Und Frauenheilkunde|September 4, 2025
Opportunities and Limitations of Modern High Throughput Sequencing in Invasive Prenatal DiagnosticsHeinz Gabriel, Markus Stumm
American Journal of Medical Genetics. Part A|April 1, 2004
Slow progression of ataxia-telangiectasia with double missense and in frame splice mutationsThilo Dörk, Regina Bendix-Waltes, Rolf-Dieter Wegner, et al.
Prenatal Diagnosis|April 21, 2012
'Normal' nuchal translucency: a justification to refrain from detailed scan? Analysis of 6858 cases with special reference to ethical aspectsRolf Becker, Lothar Schmitz, Stefania Kilavuz, et al.
Prenatal Diagnosis|February 20, 2004
Retrospective diagnosis and subsequent prenatal diagnosis of Nijmegen breakage syndromePetra Muschke, Hannswerner Gola, Raymonda Varon, et al.
The Prostate|March 3, 2004
Gain of androgen receptor gene copies in primary prostate cancer due to X chromosome polysomyAlbrecht Röpke, Andreas Erbersdobler, Peter Hammerer, et al.
Biomedicines|May 28, 2022
The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different ChromosomesAndré Weber, Thomas Liehr, Ahmed Al-Rikabi, et al.
Genes, Chromosomes & Cancer|July 18, 2006
High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11)Ilse Wieland, Petra Muschke, Marianne Volleth, et al.
European Journal of Pediatrics|November 9, 2006
Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTCSibylle Jakubiczka, Thomas Bettecken, Klaus Mohnike, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Genotype/phenotype analysis in a patient with pure and complete trisomy 12pWalter Zumkeller, Marianne Volleth, Petra Muschke, et al.
Pageof 3