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M C Vincent

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Human Reproduction (Oxford, England)|June 2, 2001
Increased aneuploidy in spermatozoa from testicular tumour patients after chemotherapy with cisplatin, etoposide and bleomycinP De Mas, M Daudin, M C Vincent, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotypeN Chassaing, P De Mas, M Tauber, et al.
Journal of Medical Genetics|April 16, 2002
Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndromeP De Mas, N Chassaing, Y Chaix, et al.
Human Gene Therapy|August 1, 1995
Adenovirus-mediated gene transfer to the respiratory tract of fetal sheep in uteroM C Vincent, B C Trapnell, R P Baughman, et al.
Genetic Counseling (Geneva, Switzerland)|September 15, 2006
A case of trisomy 12 mosaicism with pituitary malformation and polycystic ovary syndromeS Boulard, G Diene, R Barat, et al.
The British Journal of Dermatology|March 13, 2010
Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia casesN Chassaing, C Cluzeau, E Bal, et al.
Clinical Genetics|March 19, 2010
X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findingsF Clauss, N Chassaing, A Smahi, et al.
Human Molecular Genetics|September 26, 1997
Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular CenterJ Laporte, C Guiraud-Chaumeil, M C Vincent, et al.
Clinical Genetics|October 19, 2010
The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated malesD Germanaud, M Rossi, G Bussy, et al.
Scandinavian Journal of Immunology|January 5, 1999
Establishment and characterization of a human T-lymphocyte cell line immortalized by SV40 and with abnormal expression of TCR/CD3M Chatelut, S Caspar-Bauguil, J Tkaczuk, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Human Reproduction (Oxford, England)|June 2, 2001
Increased aneuploidy in spermatozoa from testicular tumour patients after chemotherapy with cisplatin, etoposide and bleomycinP De Mas, M Daudin, M C Vincent, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotypeN Chassaing, P De Mas, M Tauber, et al.
Journal of Medical Genetics|April 16, 2002
Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndromeP De Mas, N Chassaing, Y Chaix, et al.
Human Gene Therapy|August 1, 1995
Adenovirus-mediated gene transfer to the respiratory tract of fetal sheep in uteroM C Vincent, B C Trapnell, R P Baughman, et al.
Genetic Counseling (Geneva, Switzerland)|September 15, 2006
A case of trisomy 12 mosaicism with pituitary malformation and polycystic ovary syndromeS Boulard, G Diene, R Barat, et al.
The British Journal of Dermatology|March 13, 2010
Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia casesN Chassaing, C Cluzeau, E Bal, et al.
Clinical Genetics|March 19, 2010
X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findingsF Clauss, N Chassaing, A Smahi, et al.
Human Molecular Genetics|September 26, 1997
Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular CenterJ Laporte, C Guiraud-Chaumeil, M C Vincent, et al.
Clinical Genetics|October 19, 2010
The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated malesD Germanaud, M Rossi, G Bussy, et al.
Scandinavian Journal of Immunology|January 5, 1999
Establishment and characterization of a human T-lymphocyte cell line immortalized by SV40 and with abnormal expression of TCR/CD3M Chatelut, S Caspar-Bauguil, J Tkaczuk, et al.
Pageof 3