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J Feingold

Showing results (151-160 of 307) with videos related to

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Pediatric Research|April 1, 1981
Spina bifida cystica families x-ray examination and HLA typingJ P Vannier, J Lefort, B Cavelier, et al.
Human Heredity|August 7, 1998
Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in CongoJ C Bouanga, R Mouélé, C Préhu, et al.
Archives Francaises Des Maladies De L'Appareil Digestif|August 1, 1971
[Simple chemotherapy trials in 119 advanced epitheliomas of the digestive tract]P Carayon, J Feingold, Y Le Quintrec, et al.
Epilepsia|January 30, 1999
Lack of association between juvenile myoclonic epilepsy and HLA-DR13S Le Hellard, E Neidhart, P Thomas, et al.
The Journal of Allergy and Clinical Immunology|February 1, 1997
Asthma, nasal allergies, and multiple sclerosisF Neukirch, O Lyon-Caen, M Clanet, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 7, 1999
Incidence of G20210A mutation in severe vaso-occlusive events complicating sickle cell anemiaR Favier, M G Neonato, F Maillet, et al.
Journal De Genetique Humaine|October 1, 1975
[Epidemiology and genetics of ano-rectal malformations]M L Briard, J Feingold, J Kaplan, et al.
Journees Annuelles De Diabetologie De L'Hotel-Dieu|January 1, 1978
[Do genetic factors play a role in the genesis of diabetes mellitus in chronic pancreatitis?]S Lyra de Lacerda, P Bernades, J P Lenriot, et al.
Annales De Genetique|March 1, 1972
[Cytogenic and biochemical studies of 8 cases of Fanconi's anemia]J de Grouchy, C de Nava, J C Marchand, et al.
Tissue Antigens|May 1, 1980
HLA, Pi, Gm and Km phenotypes in a spina bifida population with myelo-meningoceleJ P Vannier, B Cavelier, J P Martin, et al.
Pageof 31

Showing results (151-160 of 307) with videos related to

Sort By:
Pageof 31
Pediatric Research|April 1, 1981
Spina bifida cystica families x-ray examination and HLA typingJ P Vannier, J Lefort, B Cavelier, et al.
Human Heredity|August 7, 1998
Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in CongoJ C Bouanga, R Mouélé, C Préhu, et al.
Archives Francaises Des Maladies De L'Appareil Digestif|August 1, 1971
[Simple chemotherapy trials in 119 advanced epitheliomas of the digestive tract]P Carayon, J Feingold, Y Le Quintrec, et al.
Epilepsia|January 30, 1999
Lack of association between juvenile myoclonic epilepsy and HLA-DR13S Le Hellard, E Neidhart, P Thomas, et al.
The Journal of Allergy and Clinical Immunology|February 1, 1997
Asthma, nasal allergies, and multiple sclerosisF Neukirch, O Lyon-Caen, M Clanet, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 7, 1999
Incidence of G20210A mutation in severe vaso-occlusive events complicating sickle cell anemiaR Favier, M G Neonato, F Maillet, et al.
Journal De Genetique Humaine|October 1, 1975
[Epidemiology and genetics of ano-rectal malformations]M L Briard, J Feingold, J Kaplan, et al.
Journees Annuelles De Diabetologie De L'Hotel-Dieu|January 1, 1978
[Do genetic factors play a role in the genesis of diabetes mellitus in chronic pancreatitis?]S Lyra de Lacerda, P Bernades, J P Lenriot, et al.
Annales De Genetique|March 1, 1972
[Cytogenic and biochemical studies of 8 cases of Fanconi's anemia]J de Grouchy, C de Nava, J C Marchand, et al.
Tissue Antigens|May 1, 1980
HLA, Pi, Gm and Km phenotypes in a spina bifida population with myelo-meningoceleJ P Vannier, B Cavelier, J P Martin, et al.
Pageof 31