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P Calvas

Showing results (21-30 of 71) with videos related to

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Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|April 1, 1992
[Role and contribution of karyotyping in male infertility]G Bourrouillou, L Bujan, P Calvas, et al.
Annales De Pathologie|January 1, 1987
Production of monoclonal antibodies using spleen cells from nude mice bearing human tumorsT Al Saati, A Blancher, P Calvas, et al.
Human Reproduction (Oxford, England)|December 24, 1997
Mitotic chromosomal anomalies among infertile menG Bourrouillou, P Calvas, L Bujan, et al.
Human Mutation|February 6, 1998
Novel intragenic deletions and point mutations of the ornithine transcarbamylase gene in congenital hyperammonemiaP Calvas, B Ségues, J M Rozet, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 13, 2001
Correlations between computed tomography findings and family history in otosclerotic patientsY J Shin, P Calvas, O Deguine, et al.
Scandinavian Journal of Immunology|June 3, 1999
Characterization of the three immunoglobulin G subclasses of macaquesP Calvas, P Apoil, F Fortenfant, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Chimpanzee Rh-like blood group genes map to chromosome region 1p36.1-->p34.2 by in situ hybridizationP Calvas, A Blancher, D Depétris, et al.
Clinical Genetics|June 13, 2012
Mutation analysis of the STRA6 gene in isolated and non-isolated anophthalmia/microphthalmiaN Chassaing, N Ragge, A Kariminejad, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypesM C Vincent, F Heitz, J Tricoire, et al.
Prenatal Diagnosis|February 22, 2002
Prenatal diagnosis of a lethal form of Netherton syndrome by SPINK5 mutation analysisE Bitoun, C Bodemer, J Amiel, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|April 1, 1992
[Role and contribution of karyotyping in male infertility]G Bourrouillou, L Bujan, P Calvas, et al.
Annales De Pathologie|January 1, 1987
Production of monoclonal antibodies using spleen cells from nude mice bearing human tumorsT Al Saati, A Blancher, P Calvas, et al.
Human Reproduction (Oxford, England)|December 24, 1997
Mitotic chromosomal anomalies among infertile menG Bourrouillou, P Calvas, L Bujan, et al.
Human Mutation|February 6, 1998
Novel intragenic deletions and point mutations of the ornithine transcarbamylase gene in congenital hyperammonemiaP Calvas, B Ségues, J M Rozet, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 13, 2001
Correlations between computed tomography findings and family history in otosclerotic patientsY J Shin, P Calvas, O Deguine, et al.
Scandinavian Journal of Immunology|June 3, 1999
Characterization of the three immunoglobulin G subclasses of macaquesP Calvas, P Apoil, F Fortenfant, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Chimpanzee Rh-like blood group genes map to chromosome region 1p36.1-->p34.2 by in situ hybridizationP Calvas, A Blancher, D Depétris, et al.
Clinical Genetics|June 13, 2012
Mutation analysis of the STRA6 gene in isolated and non-isolated anophthalmia/microphthalmiaN Chassaing, N Ragge, A Kariminejad, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypesM C Vincent, F Heitz, J Tricoire, et al.
Prenatal Diagnosis|February 22, 2002
Prenatal diagnosis of a lethal form of Netherton syndrome by SPINK5 mutation analysisE Bitoun, C Bodemer, J Amiel, et al.
Pageof 8