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D Lacombe

Showing results (131-140 of 225) with videos related to

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American Journal of Medical Genetics|July 24, 1998
Submicroscopic deletion of chromosome 16p13.3 in patients with Rubinstein-Taybi syndromeL Taine, C Goizet, Z Q Wen, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 23, 2010
Strategies to promote translational research within the European Organisation for Research and Treatment of Cancer (EORTC) Head and Neck Cancer Group: a report from the Translational Research SubcommitteeA Psyrri, L Licitra, D Lacombe, et al.
American Journal of Medical Genetics|April 5, 2000
1q32-q41 microdeletion with reference to Van der Woude syndrome and allied clefting entitiesC Houdayer, V Soupre, B Karcenty, et al.
Clinical Neurology and Neurosurgery|October 14, 2008
Leber's optic neuropathy associated with disseminated white matter disease: a case report and reviewF Perez, O Anne, S Debruxelles, et al.
European Journal of Medical Genetics|August 22, 2012
Blepharophimosis, ptosis, epicanthus inversus syndrome with translocation and deletion at chromosome 3q23 in a black African femaleM J Alao, A Lalèyè, F Lalya, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 1, 1994
Phase II trial of vinorelbine/doxorubicin as first-line therapy of advanced breast cancerM Spielmann, T Dorval, F Turpin, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Proteus syndrome in 7 patients: clinical and genetic considerationsD Lacombe, A Taieb, P Vergnes, et al.
Prenatal Diagnosis|September 5, 2002
Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counsellingB Gilbert, C Yardin, S Briault, et al.
European Journal of Cancer (Oxford, England : 1990)|July 2, 2002
Multicentre phase II and pharmacokinetic study of RFS2000 (9-nitro-camptothecin) administered orally 5 days a week in patients with glioblastoma multiformeE Raymond, M Campone, R Stupp, et al.
Journal of Medical Genetics|June 19, 2002
Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndromeI Coupry, C Roudaut, M Stef, et al.
Pageof 23

Showing results (131-140 of 225) with videos related to

Sort By:
Pageof 23
American Journal of Medical Genetics|July 24, 1998
Submicroscopic deletion of chromosome 16p13.3 in patients with Rubinstein-Taybi syndromeL Taine, C Goizet, Z Q Wen, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 23, 2010
Strategies to promote translational research within the European Organisation for Research and Treatment of Cancer (EORTC) Head and Neck Cancer Group: a report from the Translational Research SubcommitteeA Psyrri, L Licitra, D Lacombe, et al.
American Journal of Medical Genetics|April 5, 2000
1q32-q41 microdeletion with reference to Van der Woude syndrome and allied clefting entitiesC Houdayer, V Soupre, B Karcenty, et al.
Clinical Neurology and Neurosurgery|October 14, 2008
Leber's optic neuropathy associated with disseminated white matter disease: a case report and reviewF Perez, O Anne, S Debruxelles, et al.
European Journal of Medical Genetics|August 22, 2012
Blepharophimosis, ptosis, epicanthus inversus syndrome with translocation and deletion at chromosome 3q23 in a black African femaleM J Alao, A Lalèyè, F Lalya, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 1, 1994
Phase II trial of vinorelbine/doxorubicin as first-line therapy of advanced breast cancerM Spielmann, T Dorval, F Turpin, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Proteus syndrome in 7 patients: clinical and genetic considerationsD Lacombe, A Taieb, P Vergnes, et al.
Prenatal Diagnosis|September 5, 2002
Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counsellingB Gilbert, C Yardin, S Briault, et al.
European Journal of Cancer (Oxford, England : 1990)|July 2, 2002
Multicentre phase II and pharmacokinetic study of RFS2000 (9-nitro-camptothecin) administered orally 5 days a week in patients with glioblastoma multiformeE Raymond, M Campone, R Stupp, et al.
Journal of Medical Genetics|June 19, 2002
Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndromeI Coupry, C Roudaut, M Stef, et al.
Pageof 23