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R Siebert

Showing results (161-170 of 332) with videos related to

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Zeitschrift Fur Medizinische Laboratoriumsdiagnostik|January 1, 1986
[Model of the interpretation process in the visual analysis of orienting tests]H G Neymeyer, U Nestke, F Kretzschmar, et al.
Molecular Cytogenetics|April 11, 2026
Discrepant findings of prenatal diagnostics in a case of fetal partial trisomy 21 and fetoplacental mosaicismT Dittrich, R Wenzel, A Beck, et al.
Teratology|June 1, 1981
The facial features of holoprosencephaly in anencephalic human specimens. I. Historical review and associated malformationsR J Lemire, M M Cohen, J B Beckwith, et al.
Teratology|June 1, 1981
The facial features of holoprosencephaly in anencephalic human specimens. II. Craniofacial anatomyJ R Siebert, V G Kokich, J B Beckwith, et al.
Leukemia & Lymphoma|June 1, 1997
Recurrence of Hodgkin's disease after 10 or more years: late relapse or de-novo malignancy due to HLA-DPB1*0301-linked susceptibility?R Siebert, A Fosså, W Kaiser, et al.
Reproductive Toxicology (Elmsford, N.Y.)|December 9, 2008
Exposure to environmental tobacco smoke during pregnancy in rats yields less effect on indices of brain cell number and size than does postnatal exposureSidney M Gospe, John A Joyce, Joseph R Siebert, et al.
The Southern African Journal of Critical Care : the Official Journal of the Critical Care Society|June 26, 2023
The role of laboratory testing in hospitalised and critically ill COVID-19-positive patientsS Omar, D Baker, R Siebert, et al.
Genomics|January 27, 1998
Mapping of the gene encoding human beta-defensin-2 (DEFB2) to chromosome region 8p22-p23.1J Harder, R Siebert, Y Zhang, et al.
Cancer Genetics and Cytogenetics|May 10, 2001
No evidence for deletions of the NBS1 gene in lymphomasM Stumm, A von Ruskowsky, R Siebert, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|January 30, 2002
Agenesis of the mesencephalon and metencephalon with cerebellar hypoplasia: putative mutation in the EN2 gene--report of 2 cases in early infancyHarvey B Sarnat, Denis R Benjamin, Joseph R Siebert, et al.
Pageof 34

Showing results (161-170 of 332) with videos related to

Sort By:
Pageof 34
Zeitschrift Fur Medizinische Laboratoriumsdiagnostik|January 1, 1986
[Model of the interpretation process in the visual analysis of orienting tests]H G Neymeyer, U Nestke, F Kretzschmar, et al.
Molecular Cytogenetics|April 11, 2026
Discrepant findings of prenatal diagnostics in a case of fetal partial trisomy 21 and fetoplacental mosaicismT Dittrich, R Wenzel, A Beck, et al.
Teratology|June 1, 1981
The facial features of holoprosencephaly in anencephalic human specimens. I. Historical review and associated malformationsR J Lemire, M M Cohen, J B Beckwith, et al.
Teratology|June 1, 1981
The facial features of holoprosencephaly in anencephalic human specimens. II. Craniofacial anatomyJ R Siebert, V G Kokich, J B Beckwith, et al.
Leukemia & Lymphoma|June 1, 1997
Recurrence of Hodgkin's disease after 10 or more years: late relapse or de-novo malignancy due to HLA-DPB1*0301-linked susceptibility?R Siebert, A Fosså, W Kaiser, et al.
Reproductive Toxicology (Elmsford, N.Y.)|December 9, 2008
Exposure to environmental tobacco smoke during pregnancy in rats yields less effect on indices of brain cell number and size than does postnatal exposureSidney M Gospe, John A Joyce, Joseph R Siebert, et al.
The Southern African Journal of Critical Care : the Official Journal of the Critical Care Society|June 26, 2023
The role of laboratory testing in hospitalised and critically ill COVID-19-positive patientsS Omar, D Baker, R Siebert, et al.
Genomics|January 27, 1998
Mapping of the gene encoding human beta-defensin-2 (DEFB2) to chromosome region 8p22-p23.1J Harder, R Siebert, Y Zhang, et al.
Cancer Genetics and Cytogenetics|May 10, 2001
No evidence for deletions of the NBS1 gene in lymphomasM Stumm, A von Ruskowsky, R Siebert, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|January 30, 2002
Agenesis of the mesencephalon and metencephalon with cerebellar hypoplasia: putative mutation in the EN2 gene--report of 2 cases in early infancyHarvey B Sarnat, Denis R Benjamin, Joseph R Siebert, et al.
Pageof 34