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D Fairweather

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Hemoglobin|January 1, 1977
Prenatal diagnosis of hemoglobinopathies: detection of alpha-thalassemia trait and of sickle cell disease in uteroB P Alter, D G Nathan, C B Modell, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Assignment of genes encoding GABAA receptor subunits alpha 1, alpha 6, beta 2, and gamma 2 to a YAC contig of 5q33M Kostrzewa, A Köhler, K Eppelt, et al.
Immunology|September 19, 1998
Wild isolates of murine cytomegalovirus induce myocarditis and antibodies that cross-react with virus and cardiac myosinD Fairweather, C M Lawson, A J Chapman, et al.
Journal of Medical Genetics|March 1, 1994
X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphismsS Cochrane, J Bergoffen, N D Fairweather, et al.
Nature Immunology|July 31, 2001
Contribution of the innate immune system to autoimmune myocarditis: a role for complementZ Kaya, M Afanasyeva, Y Wang, et al.
The New England Journal of Medicine|December 23, 1976
Prenatal diagnosis of hemoglobinopathies. A review of 15 casesB P Alter, C B Modell, D Fairweather, et al.
Journal of the Electrochemical Society|December 1, 2021
Effects of Cathode Corrosion on Through-Plane Water Transport in Proton Exchange Membrane Fuel CellsJoseph D Fairweather, Dusan Spernjak, Adam Z Weber, et al.
Genomics|January 1, 1995
Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase elk to a 200-kilobasepair region in human chromosome Xq12F A Fletcher, K Huebner, L G Shaffer, et al.
Human Heredity|May 1, 1995
Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1M A Pericak-Vance, D F Barker, J A Bergoffen, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Integrated physical and transcript map of 5q31.3-qterM Kostrzewa, B W Krings, M J Dixon, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Hemoglobin|January 1, 1977
Prenatal diagnosis of hemoglobinopathies: detection of alpha-thalassemia trait and of sickle cell disease in uteroB P Alter, D G Nathan, C B Modell, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Assignment of genes encoding GABAA receptor subunits alpha 1, alpha 6, beta 2, and gamma 2 to a YAC contig of 5q33M Kostrzewa, A Köhler, K Eppelt, et al.
Immunology|September 19, 1998
Wild isolates of murine cytomegalovirus induce myocarditis and antibodies that cross-react with virus and cardiac myosinD Fairweather, C M Lawson, A J Chapman, et al.
Journal of Medical Genetics|March 1, 1994
X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphismsS Cochrane, J Bergoffen, N D Fairweather, et al.
Nature Immunology|July 31, 2001
Contribution of the innate immune system to autoimmune myocarditis: a role for complementZ Kaya, M Afanasyeva, Y Wang, et al.
The New England Journal of Medicine|December 23, 1976
Prenatal diagnosis of hemoglobinopathies. A review of 15 casesB P Alter, C B Modell, D Fairweather, et al.
Journal of the Electrochemical Society|December 1, 2021
Effects of Cathode Corrosion on Through-Plane Water Transport in Proton Exchange Membrane Fuel CellsJoseph D Fairweather, Dusan Spernjak, Adam Z Weber, et al.
Genomics|January 1, 1995
Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase elk to a 200-kilobasepair region in human chromosome Xq12F A Fletcher, K Huebner, L G Shaffer, et al.
Human Heredity|May 1, 1995
Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1M A Pericak-Vance, D F Barker, J A Bergoffen, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Integrated physical and transcript map of 5q31.3-qterM Kostrzewa, B W Krings, M J Dixon, et al.
Pageof 2