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

N Philip

Showing results (181-190 of 212) with videos related to

Pageof 22
Sort By:
Dermatology (Basel, Switzerland)|September 10, 1998
Physiopathogenic investigations in a case of familial stiff-skin syndromeM A Richard, J J Grob, N Philip, et al.
Clinical Genetics|November 15, 2005
Tetra-amelia and lung aplasia syndrome: report of a new family and exclusion of candidate genesM Krahn, S Julia, S Sigaudy, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 1998
Chronic renal failure and cranioectodermal dysplasia: a further stepM Tsimaratos, E Bérard, S Sigaudy, et al.
Diagnostic and Interventional Imaging|March 20, 2016
Prenatal diagnosis of bowel malposition using T2-weighted fetal MRI sequencesM Kheiri, E Lesieur, A Dabadie, et al.
Journal of Medical Genetics|March 8, 2003
Clinical, radiological, and chondro-osseous findings in opsismodysplasia: survey of a series of 12 unreported casesV Cormier-Daire, A L Delezoide, N Philip, et al.
Revue Neurologique|May 3, 2017
Parkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatmentB Dufournet, K Nguyen, P Charles, 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.
Journal of Medical Genetics|June 17, 2003
Is the locus for Costello syndrome on 11p?B Kerr, M L Mucchielli, S Sigaudy, et al.
Life Sciences|July 9, 2005
Access to exercise and its relation to cardiovascular health and gene expression in laboratory animalsNatalie B Schweitzer, Helaine M Alessio, Ann E Hagerman, et al.
Journal of Medical Genetics|March 4, 2005
Assignment of a new congenital fibrosis of extraocular muscles type 3 (CFEOM3) locus, FEOM4, based on a balanced translocation t(2;13) (q37.3;q12.11) and identification of candidate genesP Aubourg, M Krahn, R Bernard, et al.
Pageof 22

Showing results (181-190 of 212) with videos related to

Sort By:
Pageof 22
Dermatology (Basel, Switzerland)|September 10, 1998
Physiopathogenic investigations in a case of familial stiff-skin syndromeM A Richard, J J Grob, N Philip, et al.
Clinical Genetics|November 15, 2005
Tetra-amelia and lung aplasia syndrome: report of a new family and exclusion of candidate genesM Krahn, S Julia, S Sigaudy, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 1998
Chronic renal failure and cranioectodermal dysplasia: a further stepM Tsimaratos, E Bérard, S Sigaudy, et al.
Diagnostic and Interventional Imaging|March 20, 2016
Prenatal diagnosis of bowel malposition using T2-weighted fetal MRI sequencesM Kheiri, E Lesieur, A Dabadie, et al.
Journal of Medical Genetics|March 8, 2003
Clinical, radiological, and chondro-osseous findings in opsismodysplasia: survey of a series of 12 unreported casesV Cormier-Daire, A L Delezoide, N Philip, et al.
Revue Neurologique|May 3, 2017
Parkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatmentB Dufournet, K Nguyen, P Charles, 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.
Journal of Medical Genetics|June 17, 2003
Is the locus for Costello syndrome on 11p?B Kerr, M L Mucchielli, S Sigaudy, et al.
Life Sciences|July 9, 2005
Access to exercise and its relation to cardiovascular health and gene expression in laboratory animalsNatalie B Schweitzer, Helaine M Alessio, Ann E Hagerman, et al.
Journal of Medical Genetics|March 4, 2005
Assignment of a new congenital fibrosis of extraocular muscles type 3 (CFEOM3) locus, FEOM4, based on a balanced translocation t(2;13) (q37.3;q12.11) and identification of candidate genesP Aubourg, M Krahn, R Bernard, et al.
Pageof 22