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La Nouvelle Presse Medicale
|
December 4, 1976
[Hereditary transmission of idiopathic valvular mitral prolapse]
P Bareiss, D Christmann, J J Class, et al.
Human Genetics
|
August 1, 1993
Genetic variation in transforming growth factor alpha: possible association of BamHI polymorphism with bilateral sporadic cleft lip and palate
C Stoll, J F Qian, J Feingold, et al.
Archives Francaises De Pediatrie
|
October 1, 1991
[Congenital malformations in a series of 131,760 consecutive births during 10 years]
C Stoll, B Dott, Y Alembik, et al.
Gene
|
June 3, 1997
Cloning and analysis of MART-1/Melan-A human melanoma antigen promoter regions
L H Butterfield, T C Stoll, R Lau, et al.
American Journal of Medical Genetics
|
February 15, 1992
Ventricular extrasystoles with syncopal episodes, perodactyly, and Robin in sequence in three generations: a new inherited MCA syndrome?
C Stoll, J R Kieny, B Dott, et al.
Human Genetics
|
January 1, 1983
Reexamination of paternal age effect in Down's syndrome
M P Roth, J Feingold, A Baumgarten, et al.
European Journal of Medical Genetics
|
August 2, 2005
Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709,030 births in 12 European countries
A Wiesel, A Queisser-Luft, M Clementi, et al.
Genetic Epidemiology
|
January 1, 1988
HLA and Down syndrome (DS): parents at the origin of the nondisjunction share no more HLA-A and -B antigens with their DS child than controls
C Stoll, Y Alembik, N Armbruster, et al.
World Journal of Urology
|
November 25, 2021
Supportive therapy and complementary medicine in renal cell carcinoma
M Johannsen, C Stoll, M Raida, et al.
Clinical Genetics
|
September 1, 1985
A Weaver-like syndrome with endocrinological abnormalities in a boy and his mother
C Stoll, P Talon, L Mengus, et al.
Page
of 38
Search research articles
Search
Showing results (241-250 of 377) with videos related to
Sort By:
Page
of 38
La Nouvelle Presse Medicale
|
December 4, 1976
[Hereditary transmission of idiopathic valvular mitral prolapse]
P Bareiss, D Christmann, J J Class, et al.
Human Genetics
|
August 1, 1993
Genetic variation in transforming growth factor alpha: possible association of BamHI polymorphism with bilateral sporadic cleft lip and palate
C Stoll, J F Qian, J Feingold, et al.
Archives Francaises De Pediatrie
|
October 1, 1991
[Congenital malformations in a series of 131,760 consecutive births during 10 years]
C Stoll, B Dott, Y Alembik, et al.
Gene
|
June 3, 1997
Cloning and analysis of MART-1/Melan-A human melanoma antigen promoter regions
L H Butterfield, T C Stoll, R Lau, et al.
American Journal of Medical Genetics
|
February 15, 1992
Ventricular extrasystoles with syncopal episodes, perodactyly, and Robin in sequence in three generations: a new inherited MCA syndrome?
C Stoll, J R Kieny, B Dott, et al.
Human Genetics
|
January 1, 1983
Reexamination of paternal age effect in Down's syndrome
M P Roth, J Feingold, A Baumgarten, et al.
European Journal of Medical Genetics
|
August 2, 2005
Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709,030 births in 12 European countries
A Wiesel, A Queisser-Luft, M Clementi, et al.
Genetic Epidemiology
|
January 1, 1988
HLA and Down syndrome (DS): parents at the origin of the nondisjunction share no more HLA-A and -B antigens with their DS child than controls
C Stoll, Y Alembik, N Armbruster, et al.
World Journal of Urology
|
November 25, 2021
Supportive therapy and complementary medicine in renal cell carcinoma
M Johannsen, C Stoll, M Raida, et al.
Clinical Genetics
|
September 1, 1985
A Weaver-like syndrome with endocrinological abnormalities in a boy and his mother
C Stoll, P Talon, L Mengus, et al.
Page
of 38