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Heidemarie Neitzel

Showing results (41-50 of 54) with videos related to

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Nucleus (Austin, Tex.)|February 18, 2011
Dosage effect of zero to three functional LBR-genes in vivo and in vitroSophia Gravemann, Nele Schnipper, Hannes Meyer, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11Andreas Tzschach, Anne-Marie Bisgaard, Maria Kirchhoff, et al.
Journal of Medical Genetics|December 2, 2009
Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in humanSascha Tierling, Nicole Y Souren, Jasmin Gries, et al.
Blood|June 5, 2013
A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGTPeter M Krawitz, Britta Höchsmann, Yoshiko Murakami, et al.
Clinical Dysmorphology|September 13, 2005
Three new cases with a supernumerary ring chromosome 1Laura Rodríguez, Heike Starke, Nieves Martínez Guardia, et al.
Human Genetics|May 10, 2022
Transmission ratio distortion of mutations in the master regulator of centriole biogenesis PLK4Heidemarie Neitzel, Raymonda Varon, Sana Chughtai, et al.
European Journal of Human Genetics : EJHG|November 6, 2009
High-throughput sequencing of microdissected chromosomal regionsAnja Weise, Bernd Timmermann, Manfred Grabherr, et al.
Cell Cycle (Georgetown, Tex.)|August 23, 2011
Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephalyJuan Alberto Marchal, Mahdi Ghani, Detlev Schindler, et al.
Human Mutation|July 3, 2010
Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotypeVéronique Dutrannoy, Ilja Demuth, Ulrich Baumann, et al.
European Journal of Human Genetics : EJHG|December 3, 2009
Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencingWei Chen, Reinhard Ullmann, Claudia Langnick, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Nucleus (Austin, Tex.)|February 18, 2011
Dosage effect of zero to three functional LBR-genes in vivo and in vitroSophia Gravemann, Nele Schnipper, Hannes Meyer, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11Andreas Tzschach, Anne-Marie Bisgaard, Maria Kirchhoff, et al.
Journal of Medical Genetics|December 2, 2009
Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in humanSascha Tierling, Nicole Y Souren, Jasmin Gries, et al.
Blood|June 5, 2013
A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGTPeter M Krawitz, Britta Höchsmann, Yoshiko Murakami, et al.
Clinical Dysmorphology|September 13, 2005
Three new cases with a supernumerary ring chromosome 1Laura Rodríguez, Heike Starke, Nieves Martínez Guardia, et al.
Human Genetics|May 10, 2022
Transmission ratio distortion of mutations in the master regulator of centriole biogenesis PLK4Heidemarie Neitzel, Raymonda Varon, Sana Chughtai, et al.
European Journal of Human Genetics : EJHG|November 6, 2009
High-throughput sequencing of microdissected chromosomal regionsAnja Weise, Bernd Timmermann, Manfred Grabherr, et al.
Cell Cycle (Georgetown, Tex.)|August 23, 2011
Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephalyJuan Alberto Marchal, Mahdi Ghani, Detlev Schindler, et al.
Human Mutation|July 3, 2010
Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotypeVéronique Dutrannoy, Ilja Demuth, Ulrich Baumann, et al.
European Journal of Human Genetics : EJHG|December 3, 2009
Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencingWei Chen, Reinhard Ullmann, Claudia Langnick, et al.
Pageof 6