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A Rappold

Showing results (21-30 of 160) with videos related to

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Science in Context|September 1, 2022
Representing vulnerable populations in genetic studies: The case of the RomaVeronika Lipphardt, Gudrun A Rappold, Mihai Surdu
Endocrine Reviews|June 30, 2016
A Track Record on SHOX: From Basic Research to Complex Models and TherapyAntonio Marchini, Tsutomu Ogata, Gudrun A Rappold
Mechanisms of Development|November 7, 2012
The cellular function of srGAP3 and its role in neuronal morphogenesisClaire Bacon, Volker Endris, Gudrun A Rappold
Genomics|August 1, 1992
Assignment of the human homologue of the mouse t-complex gene TCTE3 to human chromosome 6q27G A Rappold, J Trowsdale, P Lichter
The Journal of Pediatrics|October 18, 2005
All shook up by SHOX deficiencyGudrun A Rappold, Alan Shanske, Paul Saenger
Human Mutation|October 29, 2002
The human SHOX mutation databaseBeate Niesler, Christine Fischer, Gudrun A Rappold
Genes|January 21, 2022
Disrupted Mitochondrial Network Drives Deficits of Learning and Memory in a Mouse Model of <i>FOXP1</i> HaploinsufficiencyJing Wang, Gudrun A Rappold, Henning Fröhlich
Science (New York, N.Y.)|September 23, 2021
Protect minorities in genetic researchVeronika Lipphardt, Gudrun A Rappold, Mihai Surdu
Genomics|December 1, 1993
Genetic map of the human pseudoautosomal region reveals a high rate of recombination in female meiosis at the Xp telomereA Henke, C Fischer, G A Rappold
Applied Stochastic Models in Business and Industry|March 28, 2020
Copula-based robust optimal block designsA Rappold, W G Müller, D C Woods
Pageof 16

Showing results (21-30 of 160) with videos related to

Sort By:
Pageof 16
Science in Context|September 1, 2022
Representing vulnerable populations in genetic studies: The case of the RomaVeronika Lipphardt, Gudrun A Rappold, Mihai Surdu
Endocrine Reviews|June 30, 2016
A Track Record on SHOX: From Basic Research to Complex Models and TherapyAntonio Marchini, Tsutomu Ogata, Gudrun A Rappold
Mechanisms of Development|November 7, 2012
The cellular function of srGAP3 and its role in neuronal morphogenesisClaire Bacon, Volker Endris, Gudrun A Rappold
Genomics|August 1, 1992
Assignment of the human homologue of the mouse t-complex gene TCTE3 to human chromosome 6q27G A Rappold, J Trowsdale, P Lichter
The Journal of Pediatrics|October 18, 2005
All shook up by SHOX deficiencyGudrun A Rappold, Alan Shanske, Paul Saenger
Human Mutation|October 29, 2002
The human SHOX mutation databaseBeate Niesler, Christine Fischer, Gudrun A Rappold
Genes|January 21, 2022
Disrupted Mitochondrial Network Drives Deficits of Learning and Memory in a Mouse Model of <i>FOXP1</i> HaploinsufficiencyJing Wang, Gudrun A Rappold, Henning Fröhlich
Science (New York, N.Y.)|September 23, 2021
Protect minorities in genetic researchVeronika Lipphardt, Gudrun A Rappold, Mihai Surdu
Genomics|December 1, 1993
Genetic map of the human pseudoautosomal region reveals a high rate of recombination in female meiosis at the Xp telomereA Henke, C Fischer, G A Rappold
Applied Stochastic Models in Business and Industry|March 28, 2020
Copula-based robust optimal block designsA Rappold, W G Müller, D C Woods
Pageof 16