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M Hertz

Showing results (231-240 of 392) with videos related to

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Journal of Craniofacial Genetics and Developmental Biology|January 1, 1981
New clinical observations in the trichorhinophalangeal syndromeR M Goodman, R Trilling, M Hertz, et al.
European Journal of Human Genetics : EJHG|July 6, 2000
Cathepsin K gene mutations and 1q21 haplotypes in at patients with pycnodysostosis in an outbred populationA Haagerup, J M Hertz, M F Christensen, et al.
Transplantation|April 9, 2001
Hyperacute rejection in single lung transplantation--case report of successful management by means of plasmapheresis and antithymocyte globulin treatmentH B Bittner, J Dunitz, M Hertz, et al.
Clinical Genetics|October 1, 1994
Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplicationJ M Hertz, A D Børglum, C A Brandt, et al.
Clinical Genetics|July 1, 1985
The facio-audio-symphalangism syndrome: report of a case and review of the literatureS A Hurvitz, R M Goodman, M Hertz, et al.
Science Advances|March 22, 2024
Iterative nanoparticle bioengineering enabled by x-ray fluorescence imagingGiovanni M Saladino, Bertha Brodin, Ronak Kakadiya, et al.
Abdominal Imaging|February 20, 2003
Granulomatous appendicitis presenting as right lower quadrant pain: CT findingsR Zissin, G Gayer, J Bernheim, et al.
Ugeskrift for Laeger|September 27, 2001
[The molecular genetic background of hereditary craniosynostoses and chondrodysplasias]J M Hertz, I Juncker, L Christensen, et al.
Abdominal Imaging|August 15, 2001
Iliopsoas abscess: a report of 24 patients diagnosed by CTR Zissin, G Gayer, E Kots, et al.
European Radiology|May 17, 2001
CT findings of the chest in adults with aspirated foreign bodiesR Zissin, M Shapiro-Feinberg, J Rozenman, et al.
Pageof 40

Showing results (231-240 of 392) with videos related to

Sort By:
Pageof 40
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1981
New clinical observations in the trichorhinophalangeal syndromeR M Goodman, R Trilling, M Hertz, et al.
European Journal of Human Genetics : EJHG|July 6, 2000
Cathepsin K gene mutations and 1q21 haplotypes in at patients with pycnodysostosis in an outbred populationA Haagerup, J M Hertz, M F Christensen, et al.
Transplantation|April 9, 2001
Hyperacute rejection in single lung transplantation--case report of successful management by means of plasmapheresis and antithymocyte globulin treatmentH B Bittner, J Dunitz, M Hertz, et al.
Clinical Genetics|October 1, 1994
Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplicationJ M Hertz, A D Børglum, C A Brandt, et al.
Clinical Genetics|July 1, 1985
The facio-audio-symphalangism syndrome: report of a case and review of the literatureS A Hurvitz, R M Goodman, M Hertz, et al.
Science Advances|March 22, 2024
Iterative nanoparticle bioengineering enabled by x-ray fluorescence imagingGiovanni M Saladino, Bertha Brodin, Ronak Kakadiya, et al.
Abdominal Imaging|February 20, 2003
Granulomatous appendicitis presenting as right lower quadrant pain: CT findingsR Zissin, G Gayer, J Bernheim, et al.
Ugeskrift for Laeger|September 27, 2001
[The molecular genetic background of hereditary craniosynostoses and chondrodysplasias]J M Hertz, I Juncker, L Christensen, et al.
Abdominal Imaging|August 15, 2001
Iliopsoas abscess: a report of 24 patients diagnosed by CTR Zissin, G Gayer, E Kots, et al.
European Radiology|May 17, 2001
CT findings of the chest in adults with aspirated foreign bodiesR Zissin, M Shapiro-Feinberg, J Rozenman, et al.
Pageof 40