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P Calvas

Showing results (41-50 of 71) with videos related to

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Journal of Medical Primatology|January 1, 1993
Relationship between chimpanzee Rh-like genes and the R-C-E-F blood group systemI Salvignol, A Blancher, P Calvas, et al.
Early Human Development|April 28, 2000
Lower alkaline phosphatase activity and occurrence of an abnormal hybrid intestinal/tissue non-specific isoform in Down's syndrome amniotic fluidsH Vergnes, J Grozdea, C Denier, 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.
Cancer Genetics and Cytogenetics|October 1, 1992
t(9;11)(p22;q23) translocation in blastic phase of chronic myeloid leukemiaN Dastugue, E Duchayne, F Huguet, 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.
Journal of Medical Genetics|October 5, 2001
No evidence of allelic heterogeneity in the DYT1 gene of European patients with early onset torsion dystoniaS Tuffery-Giraud, L Cavalier, A Roubertie, 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.
Human Mutation|January 1, 1996
Partial duplication [dup. TCAC (178)] and novel point mutations (T125M, G188R, A209V, and H302L) of the ornithine transcarbamylase gene in congenital hyperammonemiaB Gilbert-Dussardier, B Segues, J M Rozet, et al.
Human Mutation|January 1, 1996
A 3-base pair in-frame deletion in exon 8 (delGlu272/273) of the ornithine transcarbamylase gene in late-onset hyperammonemic comaB Ségues, P S Veber, D Rabier, et al.
Acta Neuropathologica|July 21, 1999
A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsyM B Delisle, J R Murrell, R Richardson, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
Journal of Medical Primatology|January 1, 1993
Relationship between chimpanzee Rh-like genes and the R-C-E-F blood group systemI Salvignol, A Blancher, P Calvas, et al.
Early Human Development|April 28, 2000
Lower alkaline phosphatase activity and occurrence of an abnormal hybrid intestinal/tissue non-specific isoform in Down's syndrome amniotic fluidsH Vergnes, J Grozdea, C Denier, 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.
Cancer Genetics and Cytogenetics|October 1, 1992
t(9;11)(p22;q23) translocation in blastic phase of chronic myeloid leukemiaN Dastugue, E Duchayne, F Huguet, 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.
Journal of Medical Genetics|October 5, 2001
No evidence of allelic heterogeneity in the DYT1 gene of European patients with early onset torsion dystoniaS Tuffery-Giraud, L Cavalier, A Roubertie, 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.
Human Mutation|January 1, 1996
Partial duplication [dup. TCAC (178)] and novel point mutations (T125M, G188R, A209V, and H302L) of the ornithine transcarbamylase gene in congenital hyperammonemiaB Gilbert-Dussardier, B Segues, J M Rozet, et al.
Human Mutation|January 1, 1996
A 3-base pair in-frame deletion in exon 8 (delGlu272/273) of the ornithine transcarbamylase gene in late-onset hyperammonemic comaB Ségues, P S Veber, D Rabier, et al.
Acta Neuropathologica|July 21, 1999
A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsyM B Delisle, J R Murrell, R Richardson, et al.
Pageof 8