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S Marlin

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American Journal of Medical Genetics. Part A|May 27, 2010
Fourth case of cerebral, ocular, dental, auricular, skeletal syndrome (CODAS), description of new features and molecular analysisS Marlin, H Ducou Le Pointe, M Le Merrer, et al.
Pathologie-Biologie|February 2, 2010
[Genetic testing in the context of the revision of the French law on bioethics]D Bonneau, S Marlin, D Sanlaville, et al.
Clinical Genetics|September 27, 2014
SOX10 mutations mimic isolated hearing lossV Pingault, E Faubert, V Baral, et al.
Journal of Medical Genetics|August 2, 2005
RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosaA Moore, E Escudier, G Roger, et al.
Human Mutation|October 26, 1999
Townes-Brocks syndrome: detection of a SALL1 mutation hot spot and evidence for a position effect in one patientS Marlin, S Blanchard, R Slim, et al.
Gene|July 16, 2013
Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairmentC Bonnet, M Louha, N Loundon, et al.
Clinical Genetics|September 6, 2013
Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major causeF Petit, F Escande, A S Jourdain, et al.
Journal of Clinical and Translational Science|July 2, 2025
Participant experiences in a decentralized clinical trial using digital health technologies: The ACTIV-6 studyCarrie Reale, Janelle Faiman, Russ Beebe, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 16, 2000
Phase III comparative study of vinorelbine combined with doxorubicin versus doxorubicin alone in disseminated metastatic/recurrent breast cancer: National Cancer Institute of Canada Clinical Trials Group Study MA8B Norris, K I Pritchard, K James, et al.
Journal of Medical Genetics|November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experienceB Keren, A Hadchouel, S Saba, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part A|May 27, 2010
Fourth case of cerebral, ocular, dental, auricular, skeletal syndrome (CODAS), description of new features and molecular analysisS Marlin, H Ducou Le Pointe, M Le Merrer, et al.
Pathologie-Biologie|February 2, 2010
[Genetic testing in the context of the revision of the French law on bioethics]D Bonneau, S Marlin, D Sanlaville, et al.
Clinical Genetics|September 27, 2014
SOX10 mutations mimic isolated hearing lossV Pingault, E Faubert, V Baral, et al.
Journal of Medical Genetics|August 2, 2005
RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosaA Moore, E Escudier, G Roger, et al.
Human Mutation|October 26, 1999
Townes-Brocks syndrome: detection of a SALL1 mutation hot spot and evidence for a position effect in one patientS Marlin, S Blanchard, R Slim, et al.
Gene|July 16, 2013
Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairmentC Bonnet, M Louha, N Loundon, et al.
Clinical Genetics|September 6, 2013
Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major causeF Petit, F Escande, A S Jourdain, et al.
Journal of Clinical and Translational Science|July 2, 2025
Participant experiences in a decentralized clinical trial using digital health technologies: The ACTIV-6 studyCarrie Reale, Janelle Faiman, Russ Beebe, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 16, 2000
Phase III comparative study of vinorelbine combined with doxorubicin versus doxorubicin alone in disseminated metastatic/recurrent breast cancer: National Cancer Institute of Canada Clinical Trials Group Study MA8B Norris, K I Pritchard, K James, et al.
Journal of Medical Genetics|November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experienceB Keren, A Hadchouel, S Saba, et al.
Pageof 8