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J Oostra

Showing results (41-50 of 55) with videos related to

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International Journal of Legal Medicine|December 20, 2019
Added value of post-mortem computed tomography (PMCT) to clinical findings for cause of death determination in adult "natural deaths"M E M Vester, R R van Rijn, W L J M Duijst, et al.
Surgical and Radiologic Anatomy : SRA|October 28, 2021
Midline crossing pulmonary vein: right upper lobe dual venous drainage, with partial anomalous venous return of the right lung into a persistent left superior vena cavaJ van Schuppen, A E van der Hulst, I M Kuipers, et al.
Case Reports in Obstetrics and Gynecology|January 25, 2017
Prenatal Evidence of Persistent Notochord and Absent Sacrum Caused by a Mutation in the T (Brachyury) GeneF Fontanella, M C van Maarle, P Robles de Medina, et al.
American Journal of Human Genetics|October 23, 1997
A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosomeJ J Assink, N T Tijmes, J B ten Brink, et al.
American Journal of Human Genetics|October 1, 1995
Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findingsR J Oostra, C Van den Bogert, L G Nijtmans, et al.
American Journal of Human Genetics|April 16, 1998
Reply to Hofmann et alD Mackey, R J Oostra, T Rosenberg, et al.
Biomedical Optics Express|October 3, 2017
Evaluation of collimated polarized light imaging for real-time intraoperative selective nerve identification in the human handK W T K Chin, A F Engelsman, P T K Chin, et al.
American Journal of Human Genetics|August 1, 1996
Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathyD A Mackey, R J Oostra, T Rosenberg, et al.
Forensic Science International|March 18, 2018
Dutch population specific sex estimation formulae using the proximal femurK L Colman, M C L Janssen, K E Stull, et al.
Clinical Genetics|June 1, 1997
On the many faces of Leber hereditary optic neuropathyR J Oostra, N T Tijmes, J M Cobben, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
International Journal of Legal Medicine|December 20, 2019
Added value of post-mortem computed tomography (PMCT) to clinical findings for cause of death determination in adult "natural deaths"M E M Vester, R R van Rijn, W L J M Duijst, et al.
Surgical and Radiologic Anatomy : SRA|October 28, 2021
Midline crossing pulmonary vein: right upper lobe dual venous drainage, with partial anomalous venous return of the right lung into a persistent left superior vena cavaJ van Schuppen, A E van der Hulst, I M Kuipers, et al.
Case Reports in Obstetrics and Gynecology|January 25, 2017
Prenatal Evidence of Persistent Notochord and Absent Sacrum Caused by a Mutation in the T (Brachyury) GeneF Fontanella, M C van Maarle, P Robles de Medina, et al.
American Journal of Human Genetics|October 23, 1997
A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosomeJ J Assink, N T Tijmes, J B ten Brink, et al.
American Journal of Human Genetics|October 1, 1995
Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findingsR J Oostra, C Van den Bogert, L G Nijtmans, et al.
American Journal of Human Genetics|April 16, 1998
Reply to Hofmann et alD Mackey, R J Oostra, T Rosenberg, et al.
Biomedical Optics Express|October 3, 2017
Evaluation of collimated polarized light imaging for real-time intraoperative selective nerve identification in the human handK W T K Chin, A F Engelsman, P T K Chin, et al.
American Journal of Human Genetics|August 1, 1996
Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathyD A Mackey, R J Oostra, T Rosenberg, et al.
Forensic Science International|March 18, 2018
Dutch population specific sex estimation formulae using the proximal femurK L Colman, M C L Janssen, K E Stull, et al.
Clinical Genetics|June 1, 1997
On the many faces of Leber hereditary optic neuropathyR J Oostra, N T Tijmes, J M Cobben, et al.
Pageof 6