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Peter Miny

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Therapeutische Umschau. Revue Therapeutique|October 31, 2013
[Genetic testing in the fetus and child]Deborah Bartholdi, Peter Miny
Current Opinion in Obstetrics & Gynecology|March 27, 2002
Developments in laboratory techniques for prenatal diagnosisPeter Miny, Sevgi Tercanli, Wolfgang Holzgreve
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|January 14, 2016
Increased Fetal Nuchal Translucency - Also a Risk for a Rare Submicroscopic Chromosomal AbnormalitiesSevgi Tercanli, Peter Miny, Isabel Filges
Journal of Perinatal Medicine|July 2, 2021
How genomics is changing the practice of prenatal testingIsabel Filges, Peter Miny, Wolfgang Holzgreve, et al.
Microarrays (Basel, Switzerland)|September 9, 2016
Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?Peter Miny, Friedel Wenzel, Sevgi Tercanli, et al.
Molecular Genetics & Genomic Medicine|February 27, 2020
Expanding the spectrum of SMAD3-related phenotypes to agnathia-otocephalyNicole Meier, Elisabeth Bruder, Peter Miny, et al.
Fetal and Pediatric Pathology|December 14, 2007
Upper limb amelia, facial clefts, holoprosencephaly, and interrupted aortic archAnnette Zimpfer, Peter Miny, Ulrike Dombrowski, et al.
Diagnostic Pathology|August 12, 2011
Giant ectopic liver, hepatocellular carcinoma and pachydermia-a rare genetic syndrome?Matthias Dettmer, Peter Itin, Peter Miny, et al.
American Journal of Medical Genetics. Part A|March 26, 2003
Y chromosomal polysomy: a unique case of 49,XYYYY in amniotic fluid cellsGabriele Frey-Mahn, Gabriele Behrendt, Kathrin Geiger, et al.
American Journal of Medical Genetics. Part A|October 17, 2008
Mosaic ring chromosome 8: clinical and array-CGH findings in partial trisomy 8Isabel Filges, Benno Röthlisberger, Friedel Wenzel, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Therapeutische Umschau. Revue Therapeutique|October 31, 2013
[Genetic testing in the fetus and child]Deborah Bartholdi, Peter Miny
Current Opinion in Obstetrics & Gynecology|March 27, 2002
Developments in laboratory techniques for prenatal diagnosisPeter Miny, Sevgi Tercanli, Wolfgang Holzgreve
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|January 14, 2016
Increased Fetal Nuchal Translucency - Also a Risk for a Rare Submicroscopic Chromosomal AbnormalitiesSevgi Tercanli, Peter Miny, Isabel Filges
Journal of Perinatal Medicine|July 2, 2021
How genomics is changing the practice of prenatal testingIsabel Filges, Peter Miny, Wolfgang Holzgreve, et al.
Microarrays (Basel, Switzerland)|September 9, 2016
Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?Peter Miny, Friedel Wenzel, Sevgi Tercanli, et al.
Molecular Genetics & Genomic Medicine|February 27, 2020
Expanding the spectrum of SMAD3-related phenotypes to agnathia-otocephalyNicole Meier, Elisabeth Bruder, Peter Miny, et al.
Fetal and Pediatric Pathology|December 14, 2007
Upper limb amelia, facial clefts, holoprosencephaly, and interrupted aortic archAnnette Zimpfer, Peter Miny, Ulrike Dombrowski, et al.
Diagnostic Pathology|August 12, 2011
Giant ectopic liver, hepatocellular carcinoma and pachydermia-a rare genetic syndrome?Matthias Dettmer, Peter Itin, Peter Miny, et al.
American Journal of Medical Genetics. Part A|March 26, 2003
Y chromosomal polysomy: a unique case of 49,XYYYY in amniotic fluid cellsGabriele Frey-Mahn, Gabriele Behrendt, Kathrin Geiger, et al.
American Journal of Medical Genetics. Part A|October 17, 2008
Mosaic ring chromosome 8: clinical and array-CGH findings in partial trisomy 8Isabel Filges, Benno Röthlisberger, Friedel Wenzel, et al.
Pageof 5