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C Stoll

Showing results (241-250 of 377) with videos related to

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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 palateC 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 regionsL 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 syndromeM 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 countriesA 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 controlsC Stoll, Y Alembik, N Armbruster, et al.
World Journal of Urology|November 25, 2021
Supportive therapy and complementary medicine in renal cell carcinomaM Johannsen, C Stoll, M Raida, et al.
Clinical Genetics|September 1, 1985
A Weaver-like syndrome with endocrinological abnormalities in a boy and his motherC Stoll, P Talon, L Mengus, et al.
Pageof 38

Showing results (241-250 of 377) with videos related to

Sort By:
Pageof 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 palateC 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 regionsL 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 syndromeM 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 countriesA 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 controlsC Stoll, Y Alembik, N Armbruster, et al.
World Journal of Urology|November 25, 2021
Supportive therapy and complementary medicine in renal cell carcinomaM Johannsen, C Stoll, M Raida, et al.
Clinical Genetics|September 1, 1985
A Weaver-like syndrome with endocrinological abnormalities in a boy and his motherC Stoll, P Talon, L Mengus, et al.
Pageof 38