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Pediatric Research
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April 1, 1981
Spina bifida cystica families x-ray examination and HLA typing
J P Vannier, J Lefort, B Cavelier, et al.
Human Heredity
|
August 7, 1998
Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Congo
J 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-DR13
S Le Hellard, E Neidhart, P Thomas, et al.
The Journal of Allergy and Clinical Immunology
|
February 1, 1997
Asthma, nasal allergies, and multiple sclerosis
F 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 anemia
R 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-meningocele
J P Vannier, B Cavelier, J P Martin, et al.
Page
of 31
Search research articles
Search
Showing results (151-160 of 307) with videos related to
Sort By:
Page
of 31
Pediatric Research
|
April 1, 1981
Spina bifida cystica families x-ray examination and HLA typing
J P Vannier, J Lefort, B Cavelier, et al.
Human Heredity
|
August 7, 1998
Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Congo
J 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-DR13
S Le Hellard, E Neidhart, P Thomas, et al.
The Journal of Allergy and Clinical Immunology
|
February 1, 1997
Asthma, nasal allergies, and multiple sclerosis
F 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 anemia
R 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-meningocele
J P Vannier, B Cavelier, J P Martin, et al.
Page
of 31