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M Petrou

Showing results (81-90 of 92) with videos related to

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Journal of Medical Genetics|February 1, 1986
Meiotic recombination between two polymorphic restriction sites within the beta globin gene clusterJ M Old, C Heath, A Fitches, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Audit of prenatal diagnosis for hemoglobin disorders in the United Kingdom. The first twenty yearsB Modell, M Petrou, M Layton, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|March 6, 2008
Heart transplantation for homozygous familial transthyretin (TTR) V122I cardiac amyloidosisI M Hamour, H J Lachmann, H J B Goodman, et al.
Annals of the New York Academy of Sciences|January 1, 1985
First trimester diagnosis of the hemoglobin disordersJ M Old, D J Weatherall, R H Ward, et al.
Journal of Medical Genetics|September 1, 1995
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosaM G Dunnill, C H Rodeck, A J Richards, et al.
Scandinavian Journal of Immunology|January 1, 1990
The antibody repertoire of early human B cells. I. High frequency of autoreactivity and polyreactivityP M Lydyard, R Quartey-Papafio, B Bröker, et al.
BMJ (Clinical Research Ed.)|November 5, 1997
Audit of prenatal diagnosis for haemoglobin disorders in the United Kingdom: the first 20 yearsB Modell, M Petrou, M Layton, et al.
Journal of Medical Genetics|March 1, 1994
Thalassaemia in AzerbaijanA M Kuliev, I M Rasulov, T Dadasheva, et al.
Lancet (London, England)|October 4, 1986
First-trimester fetal diagnosis for haemoglobinopathies: report on 200 casesJ M Old, A Fitches, C Heath, et al.
Academic Radiology|February 15, 2016
Diabetes, Gray Matter Loss, and Cognition in the Setting of Parkinson DiseaseM Petrou, C Davatzikos, M Hsieh, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|February 1, 1986
Meiotic recombination between two polymorphic restriction sites within the beta globin gene clusterJ M Old, C Heath, A Fitches, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Audit of prenatal diagnosis for hemoglobin disorders in the United Kingdom. The first twenty yearsB Modell, M Petrou, M Layton, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|March 6, 2008
Heart transplantation for homozygous familial transthyretin (TTR) V122I cardiac amyloidosisI M Hamour, H J Lachmann, H J B Goodman, et al.
Annals of the New York Academy of Sciences|January 1, 1985
First trimester diagnosis of the hemoglobin disordersJ M Old, D J Weatherall, R H Ward, et al.
Journal of Medical Genetics|September 1, 1995
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosaM G Dunnill, C H Rodeck, A J Richards, et al.
Scandinavian Journal of Immunology|January 1, 1990
The antibody repertoire of early human B cells. I. High frequency of autoreactivity and polyreactivityP M Lydyard, R Quartey-Papafio, B Bröker, et al.
BMJ (Clinical Research Ed.)|November 5, 1997
Audit of prenatal diagnosis for haemoglobin disorders in the United Kingdom: the first 20 yearsB Modell, M Petrou, M Layton, et al.
Journal of Medical Genetics|March 1, 1994
Thalassaemia in AzerbaijanA M Kuliev, I M Rasulov, T Dadasheva, et al.
Lancet (London, England)|October 4, 1986
First-trimester fetal diagnosis for haemoglobinopathies: report on 200 casesJ M Old, A Fitches, C Heath, et al.
Academic Radiology|February 15, 2016
Diabetes, Gray Matter Loss, and Cognition in the Setting of Parkinson DiseaseM Petrou, C Davatzikos, M Hsieh, et al.
Pageof 10