Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Feingold

Showing results (101-110 of 307) with videos related to

Pageof 31
Sort By:
European Journal of Haematology|September 1, 1993
Epidemiological and clinical study of sickle cell disease in France, French Guiana and AlgeriaM de Montalembert, M Guilloud-Bataille, J Feingold, et al.
The American Journal of Psychiatry|February 1, 1995
Gender and age at onset in schizophrenia: impact of family historyP Gorwood, M Leboyer, M Jay, et al.
Archives Francaises De Pediatrie|December 1, 1976
[Risk of recurrence of several congenital malformations: anencephaly, spina bifida, cleft palate and cleft lip]C Bonaiti-Pellie, J Feingold, M L Briard, et al.
American Journal of Medical Genetics|July 15, 1994
Is Rett syndrome a chromosome breakage syndrome?L Telvi, M Leboyer, C Chiron, et al.
Acta Haematologica|August 7, 1999
Sickle-cell disease in Brazzaville, Congo: genetical, hematological, biochemical and clinical aspectsR Mouélé, V Boukila, V Fourcade, et al.
Journal of Medical Genetics|December 1, 1984
An epidemiological and genetic study of facial clefting in France. II Segregation analysisF Demenais, C Bonaïti-Pellié, M L Briard, et al.
Human Genetics|September 22, 1977
Inbreeding in recessive diseasesP Tchen, E Bois, J Feingold, et al.
Human Genetics|February 15, 1979
Congenital glaucoma: genetic modelsF Demenais, C Bonaïti, M L Briard, et al.
Mutation Research|February 1, 1982
Activated oxygen species at the origin of chromosome breakage and sister-chromatid exchangesI Emerit, M Keck, A Levy, et al.
Humangenetik|January 1, 1974
[Genetic study of retinoblastoma (author's transl)]M L Briard-Guillemot, C Bonaïti-Pellié, J Feingold, et al.
Pageof 31

Showing results (101-110 of 307) with videos related to

Sort By:
Pageof 31
European Journal of Haematology|September 1, 1993
Epidemiological and clinical study of sickle cell disease in France, French Guiana and AlgeriaM de Montalembert, M Guilloud-Bataille, J Feingold, et al.
The American Journal of Psychiatry|February 1, 1995
Gender and age at onset in schizophrenia: impact of family historyP Gorwood, M Leboyer, M Jay, et al.
Archives Francaises De Pediatrie|December 1, 1976
[Risk of recurrence of several congenital malformations: anencephaly, spina bifida, cleft palate and cleft lip]C Bonaiti-Pellie, J Feingold, M L Briard, et al.
American Journal of Medical Genetics|July 15, 1994
Is Rett syndrome a chromosome breakage syndrome?L Telvi, M Leboyer, C Chiron, et al.
Acta Haematologica|August 7, 1999
Sickle-cell disease in Brazzaville, Congo: genetical, hematological, biochemical and clinical aspectsR Mouélé, V Boukila, V Fourcade, et al.
Journal of Medical Genetics|December 1, 1984
An epidemiological and genetic study of facial clefting in France. II Segregation analysisF Demenais, C Bonaïti-Pellié, M L Briard, et al.
Human Genetics|September 22, 1977
Inbreeding in recessive diseasesP Tchen, E Bois, J Feingold, et al.
Human Genetics|February 15, 1979
Congenital glaucoma: genetic modelsF Demenais, C Bonaïti, M L Briard, et al.
Mutation Research|February 1, 1982
Activated oxygen species at the origin of chromosome breakage and sister-chromatid exchangesI Emerit, M Keck, A Levy, et al.
Humangenetik|January 1, 1974
[Genetic study of retinoblastoma (author's transl)]M L Briard-Guillemot, C Bonaïti-Pellié, J Feingold, et al.
Pageof 31