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

C Turleau

Showing results (131-140 of 155) with videos related to

Pageof 16
Sort By:
American Journal of Medical Genetics|November 29, 2002
Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literatureS Brisset, G Joly, C Ozilou, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|March 10, 2001
[Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities]S P Romana, P Gosset, H Elghezal, et al.
Prenatal Diagnosis|April 21, 1999
Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Annales De Genetique|January 1, 1992
Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new casesM Poissonnier, C Turleau, M Olivier-Martin, et al.
Human Genetics|October 1, 1990
Investigation of three patients with the "ring syndrome", including familial transmission of ring 5, and estimation of reproductive risksK D MacDermot, E Jack, A Cooke, et al.
American Journal of Human Genetics|December 1, 1991
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndromeH J Lüdecke, C Johnson, M J Wagner, et al.
Human Genetics|July 1, 1987
Submicroscopic duplication of chromosome 21 and trisomy 21 phenotype (Down syndrome)J M Delabar, P M Sinet, B Chadefaux, et al.
Cancer Genetics and Cytogenetics|September 1, 1983
Catalase determination in various etiologic forms of Wilms' tumor and gonadoblastomaC Junien, C Turleau, G M Lenoir, et al.
Journal of Medical Genetics|May 19, 2001
Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genesA Mégarbané, M Le Lorc'H, H Elghezal, et al.
Human Reproduction (Oxford, England)|February 3, 2007
Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case reportValérie Malan, R Gesny, N Morichon-Delvallez, et al.
Pageof 16

Showing results (131-140 of 155) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics|November 29, 2002
Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literatureS Brisset, G Joly, C Ozilou, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|March 10, 2001
[Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities]S P Romana, P Gosset, H Elghezal, et al.
Prenatal Diagnosis|April 21, 1999
Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Annales De Genetique|January 1, 1992
Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new casesM Poissonnier, C Turleau, M Olivier-Martin, et al.
Human Genetics|October 1, 1990
Investigation of three patients with the "ring syndrome", including familial transmission of ring 5, and estimation of reproductive risksK D MacDermot, E Jack, A Cooke, et al.
American Journal of Human Genetics|December 1, 1991
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndromeH J Lüdecke, C Johnson, M J Wagner, et al.
Human Genetics|July 1, 1987
Submicroscopic duplication of chromosome 21 and trisomy 21 phenotype (Down syndrome)J M Delabar, P M Sinet, B Chadefaux, et al.
Cancer Genetics and Cytogenetics|September 1, 1983
Catalase determination in various etiologic forms of Wilms' tumor and gonadoblastomaC Junien, C Turleau, G M Lenoir, et al.
Journal of Medical Genetics|May 19, 2001
Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genesA Mégarbané, M Le Lorc'H, H Elghezal, et al.
Human Reproduction (Oxford, England)|February 3, 2007
Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case reportValérie Malan, R Gesny, N Morichon-Delvallez, et al.
Pageof 16