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Prenatal Diagnosis
|
October 1, 1983
Paternal age and Down's syndrome diagnosed prenatally: no association in French data
M P Roth, C Stoll, J L Taillemite, et al.
European Journal of Epidemiology
|
September 1, 1989
Risk factors in congenital heart disease
C Stoll, Y Alembik, M P Roth, et al.
BMJ (Clinical Research Ed.)
|
July 19, 2003
Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene: case control study of 492 French centenarians
Hélène Coppin, M Bensaid, S Fruchon, et al.
Journal of Neuroimmunology
|
September 1, 1995
Myelin oligodendrocyte glycoprotein (MOG) gene polymorphisms and multiple sclerosis: no evidence of disease association with MOG
M P Roth, L Dolbois, N Borot, et al.
Revue Francaise De Gynecologie Et D'Obstetrique
|
January 1, 1990
[Maternal oligo-elements and fetal malformations]
C Stoll, R Zawislak, B Dott, et al.
Gastroenterology
|
October 1, 1989
Geographic origins of Jewish patients with inflammatory bowel disease
M P Roth, G M Petersen, C McElree, et al.
Genes and Immunity
|
January 22, 2004
A vulnerability locus to multiple sclerosis maps to 7p15 in a region syntenic to an EAE locus in the rat
H Coppin, M-T Ribouchon, B Fontaine, et al.
Journal of Neuroimmunology
|
April 1, 1994
Tumor necrosis factor polymorphism in multiple sclerosis: no additional association independent of HLA
M P Roth, L Nogueira, H Coppin, et al.
Digestive Diseases and Sciences
|
June 1, 1992
Risk factors for gallstone formation during rapid loss of weight
H Yang, G M Petersen, M P Roth, et al.
Gut
|
April 1, 1993
Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews
H Yang, C McElree, M P Roth, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 97) with videos related to
Sort By:
Page
of 10
Prenatal Diagnosis
|
October 1, 1983
Paternal age and Down's syndrome diagnosed prenatally: no association in French data
M P Roth, C Stoll, J L Taillemite, et al.
European Journal of Epidemiology
|
September 1, 1989
Risk factors in congenital heart disease
C Stoll, Y Alembik, M P Roth, et al.
BMJ (Clinical Research Ed.)
|
July 19, 2003
Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene: case control study of 492 French centenarians
Hélène Coppin, M Bensaid, S Fruchon, et al.
Journal of Neuroimmunology
|
September 1, 1995
Myelin oligodendrocyte glycoprotein (MOG) gene polymorphisms and multiple sclerosis: no evidence of disease association with MOG
M P Roth, L Dolbois, N Borot, et al.
Revue Francaise De Gynecologie Et D'Obstetrique
|
January 1, 1990
[Maternal oligo-elements and fetal malformations]
C Stoll, R Zawislak, B Dott, et al.
Gastroenterology
|
October 1, 1989
Geographic origins of Jewish patients with inflammatory bowel disease
M P Roth, G M Petersen, C McElree, et al.
Genes and Immunity
|
January 22, 2004
A vulnerability locus to multiple sclerosis maps to 7p15 in a region syntenic to an EAE locus in the rat
H Coppin, M-T Ribouchon, B Fontaine, et al.
Journal of Neuroimmunology
|
April 1, 1994
Tumor necrosis factor polymorphism in multiple sclerosis: no additional association independent of HLA
M P Roth, L Nogueira, H Coppin, et al.
Digestive Diseases and Sciences
|
June 1, 1992
Risk factors for gallstone formation during rapid loss of weight
H Yang, G M Petersen, M P Roth, et al.
Gut
|
April 1, 1993
Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews
H Yang, C McElree, M P Roth, et al.
Page
of 10