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Simone Heidemann

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Journal of Genetic Counseling|November 11, 2024
First experiences with the introduction of genetic counselors in human genetic services in the German-speaking countriesSimone Heidemann, Johannes Zschocke, Gunda Schwaninger
Genetics in Medicine Open|December 23, 2024
The current state of the genetic counselor profession in the German-speaking countriesGunda Schwaninger, Simone Heidemann, Sabine Rudnik-Schöneborn, et al.
Archives of Gynecology and Obstetrics|October 11, 2017
CDH1 mutation screen in a BRCA1/2-negative familial breast-/ovarian cancer cohortFrederik Stuebs, Simone Heidemann, Almuth Caliebe, et al.
Archives of Gynecology and Obstetrics|March 2, 2018
Reply to letter by Dr. G. CorsoFrederik Stuebs, Simone Heidemann, Almuth Caliebe, et al.
Molecular Cytogenetics|December 6, 2011
Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10Jörg Weimer, Simone Heidemann, Constantin S von Kaisenberg, et al.
International Journal of Oncology|May 14, 2011
Pyrosequencing-based DNA methylation profiling of Fanconi anemia/BRCA pathway genes in laryngeal squamous cell carcinomaMarcin Szaumkessel, Julia Richter, Maciej Giefing, et al.
Journal of Perinatal Medicine|April 17, 2012
Chromosomal mosaicisms in prenatal diagnosis: correlation with first trimester screening and clinical outcomeChristel Eckmann-Scholz, Julia Mallek, Constantin S von Kaisenberg, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Prospects and challenges for the genetic counsellor profession in the German-speaking countries: report of a workshopGunda Schwaninger, Simone Heidemann, Wera Hofmann, et al.
Molecular Cytogenetics|September 7, 2010
Conflicting results of prenatal FISH with different probes for Down's Syndrome critical regions associated with mosaicism for a de novo del(21)(q22) characterised by molecular karyotyping: Case reportChristel Eckmann-Scholz, Stefan Gesk, Inga Nagel, et al.
Plos One|June 23, 2012
DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samplesChristel Eckmann-Scholz, Susanne Bens, Julia Kolarova, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Journal of Genetic Counseling|November 11, 2024
First experiences with the introduction of genetic counselors in human genetic services in the German-speaking countriesSimone Heidemann, Johannes Zschocke, Gunda Schwaninger
Genetics in Medicine Open|December 23, 2024
The current state of the genetic counselor profession in the German-speaking countriesGunda Schwaninger, Simone Heidemann, Sabine Rudnik-Schöneborn, et al.
Archives of Gynecology and Obstetrics|October 11, 2017
CDH1 mutation screen in a BRCA1/2-negative familial breast-/ovarian cancer cohortFrederik Stuebs, Simone Heidemann, Almuth Caliebe, et al.
Archives of Gynecology and Obstetrics|March 2, 2018
Reply to letter by Dr. G. CorsoFrederik Stuebs, Simone Heidemann, Almuth Caliebe, et al.
Molecular Cytogenetics|December 6, 2011
Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10Jörg Weimer, Simone Heidemann, Constantin S von Kaisenberg, et al.
International Journal of Oncology|May 14, 2011
Pyrosequencing-based DNA methylation profiling of Fanconi anemia/BRCA pathway genes in laryngeal squamous cell carcinomaMarcin Szaumkessel, Julia Richter, Maciej Giefing, et al.
Journal of Perinatal Medicine|April 17, 2012
Chromosomal mosaicisms in prenatal diagnosis: correlation with first trimester screening and clinical outcomeChristel Eckmann-Scholz, Julia Mallek, Constantin S von Kaisenberg, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Prospects and challenges for the genetic counsellor profession in the German-speaking countries: report of a workshopGunda Schwaninger, Simone Heidemann, Wera Hofmann, et al.
Molecular Cytogenetics|September 7, 2010
Conflicting results of prenatal FISH with different probes for Down's Syndrome critical regions associated with mosaicism for a de novo del(21)(q22) characterised by molecular karyotyping: Case reportChristel Eckmann-Scholz, Stefan Gesk, Inga Nagel, et al.
Plos One|June 23, 2012
DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samplesChristel Eckmann-Scholz, Susanne Bens, Julia Kolarova, et al.
Pageof 2