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R Anwar

Showing results (31-40 of 100) with videos related to

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Thrombosis and Haemostasis|November 1, 2000
Factor XIII deficiency causing mutation, Ser295Arg, in exon 7 of the factor XIIIA geneR Anwar, L Gallivan, K J Miloszewski, et al.
The British Journal of Ophthalmology|May 1, 1997
The genetics of primary open angle glaucomaA Booth, A Churchill, R Anwar, et al.
Clinical Molecular Pathology|October 1, 1996
Novel primer specific false terminations during DNA sequencing reactions: danger of inaccuracy of mutation analysis in molecular diagnosticsR Anwar, A Booth, A J Churchill, et al.
British Journal of Haematology|November 25, 1998
Splicing and missense mutations in the human FXIIIA gene causing FXIII deficiency: effects of these mutations on FXIIIA RNA processing and protein structureR Anwar, L Gallivan, K J Miloszewski, et al.
Blood|January 28, 1999
Genotype/phenotype correlations for coagulation factor XIII: specific normal polymorphisms are associated with high or low factor XIII specific activityR Anwar, L Gallivan, S D Edmonds, et al.
Journal of Biomaterials Applications|February 2, 2015
Albumin-based micro-composite drug carriers with dual chemo-agents for targeted breast cancer treatmentFarhana Abedin, Md R Anwar, Ramazan Asmatulu, et al.
The Journal of Laryngology and Otology|January 1, 1992
Chondrosarcoma of the maxillaR Anwar, J Ruddy, S Ghosh, et al.
Paediatrica Indonesiana|September 1, 1988
Hypovolemic shock complicating nephrotic syndrome in a childL Kosnadi, W Rochmanadji, A G Sumantri, et al.
The Open Orthopaedics Journal|June 2, 2017
Serial Femoral Fractures in An Amputation Stump: A Case ReportM Nannaparaju, K Annavaram, R Anwar, et al.
Molecular Pathology : MP|February 1, 1997
Male pseudohermaphroditism resulting from a novel mutation in the human steroid 5 alpha-reductase type 2 gene (SRD5A2)R Anwar, S G Gilbey, J P New, et al.
Pageof 10

Showing results (31-40 of 100) with videos related to

Sort By:
Pageof 10
Thrombosis and Haemostasis|November 1, 2000
Factor XIII deficiency causing mutation, Ser295Arg, in exon 7 of the factor XIIIA geneR Anwar, L Gallivan, K J Miloszewski, et al.
The British Journal of Ophthalmology|May 1, 1997
The genetics of primary open angle glaucomaA Booth, A Churchill, R Anwar, et al.
Clinical Molecular Pathology|October 1, 1996
Novel primer specific false terminations during DNA sequencing reactions: danger of inaccuracy of mutation analysis in molecular diagnosticsR Anwar, A Booth, A J Churchill, et al.
British Journal of Haematology|November 25, 1998
Splicing and missense mutations in the human FXIIIA gene causing FXIII deficiency: effects of these mutations on FXIIIA RNA processing and protein structureR Anwar, L Gallivan, K J Miloszewski, et al.
Blood|January 28, 1999
Genotype/phenotype correlations for coagulation factor XIII: specific normal polymorphisms are associated with high or low factor XIII specific activityR Anwar, L Gallivan, S D Edmonds, et al.
Journal of Biomaterials Applications|February 2, 2015
Albumin-based micro-composite drug carriers with dual chemo-agents for targeted breast cancer treatmentFarhana Abedin, Md R Anwar, Ramazan Asmatulu, et al.
The Journal of Laryngology and Otology|January 1, 1992
Chondrosarcoma of the maxillaR Anwar, J Ruddy, S Ghosh, et al.
Paediatrica Indonesiana|September 1, 1988
Hypovolemic shock complicating nephrotic syndrome in a childL Kosnadi, W Rochmanadji, A G Sumantri, et al.
The Open Orthopaedics Journal|June 2, 2017
Serial Femoral Fractures in An Amputation Stump: A Case ReportM Nannaparaju, K Annavaram, R Anwar, et al.
Molecular Pathology : MP|February 1, 1997
Male pseudohermaphroditism resulting from a novel mutation in the human steroid 5 alpha-reductase type 2 gene (SRD5A2)R Anwar, S G Gilbey, J P New, et al.
Pageof 10