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N Revencu

Showing results (11-20 of 29) with videos related to

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Clinical Genetics|March 16, 2018
Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedemaE Fastré, L-E Lanteigne, R Helaers, et al.
B-ENT|March 21, 2007
Orofacial clefting: update on the role of geneticsM Ghassibe, B Bayet, N Revencu, et al.
AJNR. American Journal of Neuroradiology|December 17, 2009
A novel association between RASA1 mutations and spinal arteriovenous anomaliesR Thiex, J B Mulliken, N Revencu, et al.
European Journal of Pediatrics|November 21, 2024
Four-year evaluation of neonatal cystic fibrosis screening in Southern BelgiumM Thimmesch, S Berardis, L Hanssens, et al.
Molecular Syndromology|June 27, 2013
Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb OvergrowthN Revencu, L M Boon, A Dompmartin, et al.
Molecular Syndromology|June 27, 2013
Genotypes and phenotypes of 162 families with a glomulin mutationP Brouillard, L M Boon, N Revencu, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Clinical Genetics|March 16, 2018
Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedemaE Fastré, L-E Lanteigne, R Helaers, et al.
B-ENT|March 21, 2007
Orofacial clefting: update on the role of geneticsM Ghassibe, B Bayet, N Revencu, et al.
AJNR. American Journal of Neuroradiology|December 17, 2009
A novel association between RASA1 mutations and spinal arteriovenous anomaliesR Thiex, J B Mulliken, N Revencu, et al.
European Journal of Pediatrics|November 21, 2024
Four-year evaluation of neonatal cystic fibrosis screening in Southern BelgiumM Thimmesch, S Berardis, L Hanssens, et al.
Molecular Syndromology|June 27, 2013
Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb OvergrowthN Revencu, L M Boon, A Dompmartin, et al.
Molecular Syndromology|June 27, 2013
Genotypes and phenotypes of 162 families with a glomulin mutationP Brouillard, L M Boon, N Revencu, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Pageof 3