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

D Labie

Showing results (81-90 of 212) with videos related to

Pageof 22
Sort By:
Presse Medicale (Paris, France : 1983)|February 4, 1989
[Intermediate homozygous beta-thalassemia with high fetal hemoglobin synthesis. Molecular analysis]O Cohen-Haguenauer, C Lapoumeroulie, D Labie, et al.
Nouvelle Revue Francaise D'Hematologie|July 1, 1972
[Familial case of Genova 28 (B10) Leu-Pro hemoglobin. Clinical, hematological, genetic and biochemical study of a French family]D Labie, A Bernadou, H Wajcman, et al.
British Journal of Haematology|September 1, 1982
Homozygous deletional alpha + thalassaemia associated with unequal expression of the two remaining alpha 1 genes (alpha 1A and alpha 1Q)J Pagnier, J Elion, C Lapouméroulie, et al.
European Journal of Biochemistry|May 2, 1983
Monosaccharides bound to hemoglobins in normal and diabetic individuals. Evidence for glucose, mannose and galactose as sugars released by methanolysis of the different hemoglobin componentsR Krishnamoorthy, A Cahour, J Elion, et al.
La Nouvelle Presse Medicale|July 12, 1980
[Measure of glycosylated hemoglobin A1c: its value in the control of juvenile insulin-dependent diabetes (author's transl)]J Jos, H Wajcman, D Labie, et al.
Blood|July 1, 1992
Uniparental disomy: a novel mechanism for thalassemia majorC Beldjord, I Henry, C Bennani, et al.
FEBS Letters|October 15, 1977
Structural and functional studies of Hb Rothschild beta (C3) Trp replaced by Arg. A new variant of the alpha1beta2 contactG Gacon, O Belkhodja, H Wajcman, et al.
British Journal of Haematology|November 1, 1990
Rapid detection of a Mediterranean beta (0) beta-thalassemic splice junction mutation by DNA amplification and BsaB1 mappingC Bennani, P Sebillon, R Krishnamoorthy, et al.
Biochemical and Biophysical Research Communications|September 14, 1986
Beta thalassemia due to a novel mutation in IVS 1 sequence donor site consensus sequence creating a restriction siteC Lapoumeroulie, J Pagnier, A Bank, et al.
Sangre|January 1, 1980
[Hemoglobin lepore Boston in a Spanish heterozygote (author's transl)]C Romero, H Wajcman, J R De Juanes, et al.
Pageof 22

Showing results (81-90 of 212) with videos related to

Sort By:
Pageof 22
Presse Medicale (Paris, France : 1983)|February 4, 1989
[Intermediate homozygous beta-thalassemia with high fetal hemoglobin synthesis. Molecular analysis]O Cohen-Haguenauer, C Lapoumeroulie, D Labie, et al.
Nouvelle Revue Francaise D'Hematologie|July 1, 1972
[Familial case of Genova 28 (B10) Leu-Pro hemoglobin. Clinical, hematological, genetic and biochemical study of a French family]D Labie, A Bernadou, H Wajcman, et al.
British Journal of Haematology|September 1, 1982
Homozygous deletional alpha + thalassaemia associated with unequal expression of the two remaining alpha 1 genes (alpha 1A and alpha 1Q)J Pagnier, J Elion, C Lapouméroulie, et al.
European Journal of Biochemistry|May 2, 1983
Monosaccharides bound to hemoglobins in normal and diabetic individuals. Evidence for glucose, mannose and galactose as sugars released by methanolysis of the different hemoglobin componentsR Krishnamoorthy, A Cahour, J Elion, et al.
La Nouvelle Presse Medicale|July 12, 1980
[Measure of glycosylated hemoglobin A1c: its value in the control of juvenile insulin-dependent diabetes (author's transl)]J Jos, H Wajcman, D Labie, et al.
Blood|July 1, 1992
Uniparental disomy: a novel mechanism for thalassemia majorC Beldjord, I Henry, C Bennani, et al.
FEBS Letters|October 15, 1977
Structural and functional studies of Hb Rothschild beta (C3) Trp replaced by Arg. A new variant of the alpha1beta2 contactG Gacon, O Belkhodja, H Wajcman, et al.
British Journal of Haematology|November 1, 1990
Rapid detection of a Mediterranean beta (0) beta-thalassemic splice junction mutation by DNA amplification and BsaB1 mappingC Bennani, P Sebillon, R Krishnamoorthy, et al.
Biochemical and Biophysical Research Communications|September 14, 1986
Beta thalassemia due to a novel mutation in IVS 1 sequence donor site consensus sequence creating a restriction siteC Lapoumeroulie, J Pagnier, A Bank, et al.
Sangre|January 1, 1980
[Hemoglobin lepore Boston in a Spanish heterozygote (author's transl)]C Romero, H Wajcman, J R De Juanes, et al.
Pageof 22