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Jens Michael Hertz

Showing results (1-10 of 80) with videos related to

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Ugeskrift for Laeger|November 15, 2014
[In Process Citation]Jens Michael Hertz
Danish Medical Bulletin|September 5, 2009
Alport syndrome. Molecular genetic aspectsJens Michael Hertz
Ugeskrift for Laeger|May 17, 2005
[Cerebral palsy--what is the influence of genetic factors?]Gija Rackauskaite, Thomas Balslev, Jens Michael Hertz
Ugeskrift for Laeger|October 9, 2014
[New classification and genetic background of inherited ichthyoses]Rikke Elkjær Andersen, Jens Michael Hertz, Anette Bygum
Ugeskrift for Laeger|October 29, 2014
[Strategies for diagnosis and biochemical control of porphyrias]Axel Brock, Lars Melholt Rasmussen, Jens Michael Hertz
European Journal of Human Genetics : EJHG|December 15, 2011
Clinical utility gene card for: Alport syndromeJens Michael Hertz, Mads Thomassen, Helen Storey, et al.
Human Genetics|September 1, 2005
Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the X-chromosome comprising exon 9 through 51 of the COL4A5 geneJens Michael Hertz, Ulf Persson, Inger Juncker, et al.
European Journal of Human Genetics : EJHG|November 13, 2014
Clinical utility gene card for: Alport syndrome - update 2014Jens Michael Hertz, Mads Thomassen, Helen Storey, et al.
BMJ Case Reports|April 28, 2016
Newborn with severe epidermolysis bullosa: to treat or not to treat?Martin Lehmann Boesen, Anette Bygum, Jens Michael Hertz, et al.
Neurology|May 11, 2005
LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotypeMarianne Schwartz, Jens Michael Hertz, Marie Louise Sveen, et al.
Pageof 8

Showing results (1-10 of 80) with videos related to

Sort By:
Pageof 8
Ugeskrift for Laeger|November 15, 2014
[In Process Citation]Jens Michael Hertz
Danish Medical Bulletin|September 5, 2009
Alport syndrome. Molecular genetic aspectsJens Michael Hertz
Ugeskrift for Laeger|May 17, 2005
[Cerebral palsy--what is the influence of genetic factors?]Gija Rackauskaite, Thomas Balslev, Jens Michael Hertz
Ugeskrift for Laeger|October 9, 2014
[New classification and genetic background of inherited ichthyoses]Rikke Elkjær Andersen, Jens Michael Hertz, Anette Bygum
Ugeskrift for Laeger|October 29, 2014
[Strategies for diagnosis and biochemical control of porphyrias]Axel Brock, Lars Melholt Rasmussen, Jens Michael Hertz
European Journal of Human Genetics : EJHG|December 15, 2011
Clinical utility gene card for: Alport syndromeJens Michael Hertz, Mads Thomassen, Helen Storey, et al.
Human Genetics|September 1, 2005
Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the X-chromosome comprising exon 9 through 51 of the COL4A5 geneJens Michael Hertz, Ulf Persson, Inger Juncker, et al.
European Journal of Human Genetics : EJHG|November 13, 2014
Clinical utility gene card for: Alport syndrome - update 2014Jens Michael Hertz, Mads Thomassen, Helen Storey, et al.
BMJ Case Reports|April 28, 2016
Newborn with severe epidermolysis bullosa: to treat or not to treat?Martin Lehmann Boesen, Anette Bygum, Jens Michael Hertz, et al.
Neurology|May 11, 2005
LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotypeMarianne Schwartz, Jens Michael Hertz, Marie Louise Sveen, et al.
Pageof 8