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 Lacombe

Showing results (111-120 of 225) with videos related to

Pageof 23
Sort By:
Biochimica Et Biophysica Acta|May 3, 2016
AGC1/2, the mitochondrial aspartate-glutamate carriersN D Amoedo, G Punzi, E Obre, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|June 1, 2016
The European Organization for Research and Treatment for Cancer (EORTC) strategy for quality assurance in surgical clinical research: Assessment of the past and moving towards the futureE Tanis, C Caballero, L Collette, et al.
Brain & Development|January 11, 2000
Schizencephaly: clinical and imaging features in 30 infantile casesD Denis, J F Chateil, M Brun, et al.
Journal of Human Hypertension|April 23, 2002
Successful laparoscopic operation of bilateral pheochromocytoma in a patient with Beckwith-Wiedemann syndromeL Bémurat, P Gosse, P Ballanger, et al.
Journal of Medical Genetics|May 6, 2008
Contribution of PTEN large rearrangements in Cowden disease: a multiplex amplifiable probe hybridisation (MAPH) screening approachF Chibon, C Primois, J-M Bressieux, et al.
Neuropediatrics|July 4, 2007
Bardet-biedl syndrome and brain abnormalitiesC Rooryck, S Pelras, J-F Chateil, et al.
European Journal of Pediatrics|January 1, 1993
Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literatureA Verloes, C Elmer, D Lacombe, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
"C" trigonocephaly syndrome with diaphragmnatic herniaM C Addor, D Stefanutti, F Farron, et al.
American Journal of Medical Genetics. Part A|June 27, 2015
Homozygous 16p13.11 duplication associated with mild intellectual disability and urinary tract malformations in two siblings born from consanguineous parentsN Houcinat, B Llanas, S Moutton, et al.
American Journal of Medical Genetics|December 20, 2000
Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISHC Goizet, E Excoffier, L Taine, et al.
Pageof 23

Showing results (111-120 of 225) with videos related to

Sort By:
Pageof 23
Biochimica Et Biophysica Acta|May 3, 2016
AGC1/2, the mitochondrial aspartate-glutamate carriersN D Amoedo, G Punzi, E Obre, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|June 1, 2016
The European Organization for Research and Treatment for Cancer (EORTC) strategy for quality assurance in surgical clinical research: Assessment of the past and moving towards the futureE Tanis, C Caballero, L Collette, et al.
Brain & Development|January 11, 2000
Schizencephaly: clinical and imaging features in 30 infantile casesD Denis, J F Chateil, M Brun, et al.
Journal of Human Hypertension|April 23, 2002
Successful laparoscopic operation of bilateral pheochromocytoma in a patient with Beckwith-Wiedemann syndromeL Bémurat, P Gosse, P Ballanger, et al.
Journal of Medical Genetics|May 6, 2008
Contribution of PTEN large rearrangements in Cowden disease: a multiplex amplifiable probe hybridisation (MAPH) screening approachF Chibon, C Primois, J-M Bressieux, et al.
Neuropediatrics|July 4, 2007
Bardet-biedl syndrome and brain abnormalitiesC Rooryck, S Pelras, J-F Chateil, et al.
European Journal of Pediatrics|January 1, 1993
Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literatureA Verloes, C Elmer, D Lacombe, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
"C" trigonocephaly syndrome with diaphragmnatic herniaM C Addor, D Stefanutti, F Farron, et al.
American Journal of Medical Genetics. Part A|June 27, 2015
Homozygous 16p13.11 duplication associated with mild intellectual disability and urinary tract malformations in two siblings born from consanguineous parentsN Houcinat, B Llanas, S Moutton, et al.
American Journal of Medical Genetics|December 20, 2000
Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISHC Goizet, E Excoffier, L Taine, et al.
Pageof 23