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

B Grandchamp

Showing results (121-130 of 134) with videos related to

Pageof 14
Sort By:
Blood|April 1, 1996
The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemiaS Raynaud, H Cave, M Baens, et al.
The Journal of Clinical Investigation|November 1, 1990
Two different point G to A mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyriaM H Delfau, C Picat, F W de Rooij, et al.
European Journal of Clinical Investigation|June 12, 2001
Association studies between haemochromatosis gene mutations and the risk of cardiovascular diseasesG Hetet, A Elbaz, J Gariepy, et al.
The New England Journal of Medicine|August 27, 1998
Clinical significance of minimal residual disease in childhood acute lymphoblastic leukemia. European Organization for Research and Treatment of Cancer--Childhood Leukemia Cooperative GroupH Cavé, J van der Werff ten Bosch, S Suciu, et al.
Lancet (London, England)|September 26, 1987
DNA polymorphism of human porphobilinogen deaminase gene in acute intermittent porphyriaD H Llewellyn, G H Elder, N A Kalsheker, et al.
Blood|March 7, 1998
Neonatal hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basisJ Lamoril, H Puy, L Gouya, et al.
Cancer Genetics and Cytogenetics|September 1, 1990
Chronic myeloid leukemia with unusual variant Ph translocation (22;22)(q11;q13). Two cases with chimeric BCR-ABL transcriptsJ L Laï, Z Aissaoui, C Collyn-d'Hooghe, et al.
The British Journal of Dermatology|August 23, 2008
Xeroderma pigmentosum group C in a French Caucasian patient with multiple melanoma and unusual long-term survivalS Jacobelli, N Soufir, J J Lacapere, et al.
Annales De Genetique|January 1, 1997
Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded childrenB Gérard, M F Le Heuzey, G Brunie, et al.
The British Journal of Dermatology|January 3, 2013
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type CS Hadj-Rabia, D Oriot, N Soufir, et al.
Pageof 14

Showing results (121-130 of 134) with videos related to

Sort By:
Pageof 14
Blood|April 1, 1996
The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemiaS Raynaud, H Cave, M Baens, et al.
The Journal of Clinical Investigation|November 1, 1990
Two different point G to A mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyriaM H Delfau, C Picat, F W de Rooij, et al.
European Journal of Clinical Investigation|June 12, 2001
Association studies between haemochromatosis gene mutations and the risk of cardiovascular diseasesG Hetet, A Elbaz, J Gariepy, et al.
The New England Journal of Medicine|August 27, 1998
Clinical significance of minimal residual disease in childhood acute lymphoblastic leukemia. European Organization for Research and Treatment of Cancer--Childhood Leukemia Cooperative GroupH Cavé, J van der Werff ten Bosch, S Suciu, et al.
Lancet (London, England)|September 26, 1987
DNA polymorphism of human porphobilinogen deaminase gene in acute intermittent porphyriaD H Llewellyn, G H Elder, N A Kalsheker, et al.
Blood|March 7, 1998
Neonatal hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basisJ Lamoril, H Puy, L Gouya, et al.
Cancer Genetics and Cytogenetics|September 1, 1990
Chronic myeloid leukemia with unusual variant Ph translocation (22;22)(q11;q13). Two cases with chimeric BCR-ABL transcriptsJ L Laï, Z Aissaoui, C Collyn-d'Hooghe, et al.
The British Journal of Dermatology|August 23, 2008
Xeroderma pigmentosum group C in a French Caucasian patient with multiple melanoma and unusual long-term survivalS Jacobelli, N Soufir, J J Lacapere, et al.
Annales De Genetique|January 1, 1997
Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded childrenB Gérard, M F Le Heuzey, G Brunie, et al.
The British Journal of Dermatology|January 3, 2013
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type CS Hadj-Rabia, D Oriot, N Soufir, et al.
Pageof 14