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C Dubourg

Showing results (11-20 of 28) with videos related to

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American Journal of Medical Genetics. Part A|April 23, 2004
Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehogLivia Garavelli, C Zanacca, G Caselli, et al.
Human Mutation|January 1, 1995
French CF family genotype analysis shows that the R297Q mutation is a rare polymorphismI Dorval, P Jézéquel, B Chauvel, et al.
Molecular Human Reproduction|December 2, 2000
Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutationsP Jézéquel, C Dubourg, D Le Lannou, et al.
British Journal of Cancer|September 17, 2009
Absence of VHL gene alteration and high VEGF expression are associated with tumour aggressiveness and poor survival of renal-cell carcinomaJ-J Patard, N Rioux-Leclercq, D Masson, et al.
Medical and Pediatric Oncology|July 24, 2001
Genomic and allelic expression status of the p73 gene in human neuroblastomaM Barrois, M K Eychenne, M J Terrier-Lacombe, et al.
Clinical Genetics|January 11, 2016
Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencingC Mouden, C Dubourg, W Carré, et al.
Journal of Medical Genetics|September 25, 2008
2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?S Jaillard, C Dubourg, M Gérard-Blanluet, et al.
Human Molecular Genetics|April 4, 2001
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombinationL Y Brown, S Odent, V David, et al.
Journal of Medical Genetics|October 4, 2005
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotypeC Bendavid, B R Haddad, A Griffin, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|October 6, 1998
[Oncogenic factors of metastatic dissemination in neuroblastoma]J Da Silva, N Duarte, D Cappellen, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|April 23, 2004
Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehogLivia Garavelli, C Zanacca, G Caselli, et al.
Human Mutation|January 1, 1995
French CF family genotype analysis shows that the R297Q mutation is a rare polymorphismI Dorval, P Jézéquel, B Chauvel, et al.
Molecular Human Reproduction|December 2, 2000
Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutationsP Jézéquel, C Dubourg, D Le Lannou, et al.
British Journal of Cancer|September 17, 2009
Absence of VHL gene alteration and high VEGF expression are associated with tumour aggressiveness and poor survival of renal-cell carcinomaJ-J Patard, N Rioux-Leclercq, D Masson, et al.
Medical and Pediatric Oncology|July 24, 2001
Genomic and allelic expression status of the p73 gene in human neuroblastomaM Barrois, M K Eychenne, M J Terrier-Lacombe, et al.
Clinical Genetics|January 11, 2016
Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencingC Mouden, C Dubourg, W Carré, et al.
Journal of Medical Genetics|September 25, 2008
2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?S Jaillard, C Dubourg, M Gérard-Blanluet, et al.
Human Molecular Genetics|April 4, 2001
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombinationL Y Brown, S Odent, V David, et al.
Journal of Medical Genetics|October 4, 2005
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotypeC Bendavid, B R Haddad, A Griffin, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|October 6, 1998
[Oncogenic factors of metastatic dissemination in neuroblastoma]J Da Silva, N Duarte, D Cappellen, et al.
Pageof 3