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Friedel Wenzel

Showing results (11-20 of 25) with videos related to

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Prenatal Diagnosis|February 26, 2011
aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosisIsabel Filges, Anjeung Kang, Vanessa Klug, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|June 28, 2011
Fetal polydactyly: a study of 24 cases ascertained by prenatal sonographyIsabel Filges, Anjeung Kang, Jürgen Hench, et al.
Virchows Archiv : an International Journal of Pathology|January 25, 2017
Sharing of a PTPN11 mutation by myelodysplastic bone marrow and a mature plasmacytoid dendritic cell proliferation provides evidence for their common myelomonocytic originAndrea Bodmer, Thomas Menter, Darius Juskevicius, et al.
Leukemia & Lymphoma|December 5, 2017
Clonogenic versus morphogenic mutations in myeloid neoplasms: chronologic observations in a U2AF1, TET2, CSF3R and JAK2 'co-mutated' myeloproliferative neoplasm suggest a hierarchical order of mutations and potential predictive value for kinase inhibitor treatment responseMagdalena M Gerlach, Pontus Lundberg, Joerg Halter, et al.
Swiss Medical Weekly|February 28, 2013
First successful pregnancy in Switzerland after prospective sex determination of the embryo through the separation of X-chromosome bearing spermatozoaChristian De Geyter, Oliver Sterthaus, Peter Miny, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|November 6, 2018
RUNX1 Mutations Can Lead to Aberrant Expression of CD79a and PAX5 in Acute Myelogenous Leukemias: A Potential Diagnostic PitfallThomas Menter, Pontus Lundberg, Friedel Wenzel, et al.
Genes, Chromosomes & Cancer|July 15, 2015
Somatic alterations in juvenile polyps from BMPR1A and SMAD4 mutation carriersRobert H E Blatter, Martina Plasilova, Friedel Wenzel, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndromeIsabel Filges, Benno Röthlisberger, Nemya Boesch, et al.
Fertility and Sterility|August 27, 2011
A novel missense mutation in the high mobility group domain of SRY drastically reduces its DNA-binding capacity and causes paternally transmitted 46,XY complete gonadal dysgenesisIsabel Filges, Christophe Kunz, Peter Miny, et al.
Plos One|July 9, 2011
Discordant gene expression signatures and related phenotypic differences in lamin A- and A/C-related Hutchinson-Gilford progeria syndrome (HGPS)Martina Plasilova, Chandon Chattopadhyay, Apurba Ghosh, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Prenatal Diagnosis|February 26, 2011
aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosisIsabel Filges, Anjeung Kang, Vanessa Klug, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|June 28, 2011
Fetal polydactyly: a study of 24 cases ascertained by prenatal sonographyIsabel Filges, Anjeung Kang, Jürgen Hench, et al.
Virchows Archiv : an International Journal of Pathology|January 25, 2017
Sharing of a PTPN11 mutation by myelodysplastic bone marrow and a mature plasmacytoid dendritic cell proliferation provides evidence for their common myelomonocytic originAndrea Bodmer, Thomas Menter, Darius Juskevicius, et al.
Leukemia & Lymphoma|December 5, 2017
Clonogenic versus morphogenic mutations in myeloid neoplasms: chronologic observations in a U2AF1, TET2, CSF3R and JAK2 'co-mutated' myeloproliferative neoplasm suggest a hierarchical order of mutations and potential predictive value for kinase inhibitor treatment responseMagdalena M Gerlach, Pontus Lundberg, Joerg Halter, et al.
Swiss Medical Weekly|February 28, 2013
First successful pregnancy in Switzerland after prospective sex determination of the embryo through the separation of X-chromosome bearing spermatozoaChristian De Geyter, Oliver Sterthaus, Peter Miny, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|November 6, 2018
RUNX1 Mutations Can Lead to Aberrant Expression of CD79a and PAX5 in Acute Myelogenous Leukemias: A Potential Diagnostic PitfallThomas Menter, Pontus Lundberg, Friedel Wenzel, et al.
Genes, Chromosomes & Cancer|July 15, 2015
Somatic alterations in juvenile polyps from BMPR1A and SMAD4 mutation carriersRobert H E Blatter, Martina Plasilova, Friedel Wenzel, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndromeIsabel Filges, Benno Röthlisberger, Nemya Boesch, et al.
Fertility and Sterility|August 27, 2011
A novel missense mutation in the high mobility group domain of SRY drastically reduces its DNA-binding capacity and causes paternally transmitted 46,XY complete gonadal dysgenesisIsabel Filges, Christophe Kunz, Peter Miny, et al.
Plos One|July 9, 2011
Discordant gene expression signatures and related phenotypic differences in lamin A- and A/C-related Hutchinson-Gilford progeria syndrome (HGPS)Martina Plasilova, Chandon Chattopadhyay, Apurba Ghosh, et al.
Pageof 3