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 Badens

Showing results (21-30 of 27) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 27 results.
Presse Medicale (Paris, France : 1983)|February 3, 1996
[Genetic hemoglobin diseases. Prevention at centers for family planning and education of maternal-child protection in Marseille]D Lena-Russo, N Erny, F Serradimigni, et al.
Journal of Clinical Pathology|December 24, 2008
Neonatal screening for sickle cell disease in FranceJ Bardakdjian-Michau, M Bahuau, D Hurtrel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 9, 2020
Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature reviewJ Chavany, A Cano, B Roquelaure, et al.
Clinical Genetics|July 4, 2006
Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndromeC Badens, C Lacoste, N Philip, et al.
La Revue De Medecine Interne|March 22, 2024
[Health status and quality of life in β-thalassemia adults in Marseille, France]C Soubrier, E Jean, B De Sainte Marie, et al.
Frontiers in Physiology|August 25, 2022
New KCNN4 Variants Associated With Anemia: Stomatocytosis Without Erythrocyte DehydrationB Allegrini, S Jedele, L David Nguyen, et al.
Orphanet Journal of Rare Diseases|April 20, 2022
Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)H Mosbah, B Donadille, C Vatier, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Presse Medicale (Paris, France : 1983)|February 3, 1996
[Genetic hemoglobin diseases. Prevention at centers for family planning and education of maternal-child protection in Marseille]D Lena-Russo, N Erny, F Serradimigni, et al.
Journal of Clinical Pathology|December 24, 2008
Neonatal screening for sickle cell disease in FranceJ Bardakdjian-Michau, M Bahuau, D Hurtrel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 9, 2020
Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature reviewJ Chavany, A Cano, B Roquelaure, et al.
Clinical Genetics|July 4, 2006
Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndromeC Badens, C Lacoste, N Philip, et al.
La Revue De Medecine Interne|March 22, 2024
[Health status and quality of life in β-thalassemia adults in Marseille, France]C Soubrier, E Jean, B De Sainte Marie, et al.
Frontiers in Physiology|August 25, 2022
New KCNN4 Variants Associated With Anemia: Stomatocytosis Without Erythrocyte DehydrationB Allegrini, S Jedele, L David Nguyen, et al.
Orphanet Journal of Rare Diseases|April 20, 2022
Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)H Mosbah, B Donadille, C Vatier, et al.
Pageof 3