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Showing results (151-160 of 162) with videos related to

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Clinical Genetics|October 12, 2001
Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotypeG Joly, J M Lapierre, C Ozilou, et al.
Prenatal Diagnosis|June 22, 2000
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann featuresS Fert-Ferrer, A Guichet, J Tantau, et al.
Oncogene|March 10, 2009
Intermediate-conductance Ca2+-activated K+ channels (IKCa1) regulate human prostate cancer cell proliferation through a close control of calcium entryH Lallet-Daher, M Roudbaraki, A Bavencoffe, et al.
Journal of Medical Genetics|June 17, 2003
Spectrum of NSD1 mutations in Sotos and Weaver syndromesM Rio, L Clech, J Amiel, et al.
American Journal of Human Genetics|October 12, 2001
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structuresJ Amiel, Y Espinosa-Parrilla, J Steffann, et al.
Journal of Medical Genetics|April 16, 2002
Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardationM Rio, F Molinari, S Heuertz, et al.
Revue Des Maladies Respiratoires|February 20, 2022
[RESPIRenT: Pneumology network of innovation and translational research, a second wind for J2R]I Annesi-Maesano, P Bonniaud, G Bouchaud, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardationL Colleaux, M Rio, S Heuertz, et al.
Revue Des Maladies Respiratoires|May 24, 2021
[Tonnerre de Brest! 2020 Respiratory Research Days like no others…]I Annesi-Maesano, P Bonniaud, G Bouchaud, et al.
Revue Des Maladies Respiratoires|March 19, 2026
[The 2025 respiratory research days: A first in Caen!]I Annesi-Maesano, P Bonniaud, G Bouchaud, et al.
Pageof 17

Showing results (151-160 of 162) with videos related to

Sort By:
Pageof 17
Clinical Genetics|October 12, 2001
Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotypeG Joly, J M Lapierre, C Ozilou, et al.
Prenatal Diagnosis|June 22, 2000
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann featuresS Fert-Ferrer, A Guichet, J Tantau, et al.
Oncogene|March 10, 2009
Intermediate-conductance Ca2+-activated K+ channels (IKCa1) regulate human prostate cancer cell proliferation through a close control of calcium entryH Lallet-Daher, M Roudbaraki, A Bavencoffe, et al.
Journal of Medical Genetics|June 17, 2003
Spectrum of NSD1 mutations in Sotos and Weaver syndromesM Rio, L Clech, J Amiel, et al.
American Journal of Human Genetics|October 12, 2001
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structuresJ Amiel, Y Espinosa-Parrilla, J Steffann, et al.
Journal of Medical Genetics|April 16, 2002
Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardationM Rio, F Molinari, S Heuertz, et al.
Revue Des Maladies Respiratoires|February 20, 2022
[RESPIRenT: Pneumology network of innovation and translational research, a second wind for J2R]I Annesi-Maesano, P Bonniaud, G Bouchaud, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardationL Colleaux, M Rio, S Heuertz, et al.
Revue Des Maladies Respiratoires|May 24, 2021
[Tonnerre de Brest! 2020 Respiratory Research Days like no others…]I Annesi-Maesano, P Bonniaud, G Bouchaud, et al.
Revue Des Maladies Respiratoires|March 19, 2026
[The 2025 respiratory research days: A first in Caen!]I Annesi-Maesano, P Bonniaud, G Bouchaud, et al.
Pageof 17