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

M Goossens

Showing results (351-360 of 364) with videos related to

Pageof 37
Sort By:
Reproductive Biomedicine Online|November 26, 2011
Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertilityN Guediche, L Tosca, A Kara Terki, et al.
Molecular Psychiatry|April 19, 2021
Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disordersE El Khouri, J Ghoumid, D Haye, et al.
Physiological Measurement|July 22, 2008
Non-invasive measurement of intra-abdominal pressure: a preliminary studyG H van Ramshorst, J F Lange, R H M Goossens, et al.
British Journal of Cancer|April 25, 2007
Patients with an unexplained microsatellite instable tumour have a low risk of familial cancerL I H Overbeek, C M Kets, K M Hebeda, et al.
Neuron|March 31, 2005
Increased noise level of purkinje cell activities minimizes impact of their modulation during sensorimotor controlF E Hoebeek, J S Stahl, A M van Alphen, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutationsI Mansour, V Delague, C Cazeneuve, et al.
American Journal of Human Genetics|April 14, 2000
Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brainR L Touraine, T Attié-Bitach, E Manceau, et al.
Nature Genetics|February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung diseaseV Pingault, N Bondurand, K Kuhlbrodt, et al.
European Journal of Medical Genetics|February 4, 2014
SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplicationA Briand-Suleau, J Martinovic, L Tosca, et al.
Human Mutation|April 3, 2007
Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung diseaseL de Pontual, A Pelet, M Clement-Ziza, et al.
Pageof 37

Showing results (351-360 of 364) with videos related to

Sort By:
Pageof 37
Reproductive Biomedicine Online|November 26, 2011
Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertilityN Guediche, L Tosca, A Kara Terki, et al.
Molecular Psychiatry|April 19, 2021
Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disordersE El Khouri, J Ghoumid, D Haye, et al.
Physiological Measurement|July 22, 2008
Non-invasive measurement of intra-abdominal pressure: a preliminary studyG H van Ramshorst, J F Lange, R H M Goossens, et al.
British Journal of Cancer|April 25, 2007
Patients with an unexplained microsatellite instable tumour have a low risk of familial cancerL I H Overbeek, C M Kets, K M Hebeda, et al.
Neuron|March 31, 2005
Increased noise level of purkinje cell activities minimizes impact of their modulation during sensorimotor controlF E Hoebeek, J S Stahl, A M van Alphen, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutationsI Mansour, V Delague, C Cazeneuve, et al.
American Journal of Human Genetics|April 14, 2000
Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brainR L Touraine, T Attié-Bitach, E Manceau, et al.
Nature Genetics|February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung diseaseV Pingault, N Bondurand, K Kuhlbrodt, et al.
European Journal of Medical Genetics|February 4, 2014
SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplicationA Briand-Suleau, J Martinovic, L Tosca, et al.
Human Mutation|April 3, 2007
Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung diseaseL de Pontual, A Pelet, M Clement-Ziza, et al.
Pageof 37