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C Templado

Showing results (11-20 of 57) with videos related to

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Human Reproduction (Oxford, England)|October 1, 1987
Synaptonemal complex studies in the maleF Vidal, J Navarro, C Templado, et al.
Molecular Reproduction and Development|June 1, 1990
Effect of culture conditions and media on the frequency of chromosomal abnormalities in human sperm chromosome complementsR H Martin, C Templado, E Ko, et al.
Human Genetics|January 1, 1980
Meiotic studies in human semen. Report of 180 casesC Templado, S Marina, M D Coll, et al.
Human Genetics|April 3, 2001
Numerical chromosome abnormalities in the spermatozoa of the fathers of children with trisomy 21 of paternal origin: generalised tendency to meiotic non-disjunctionS R Soares, C Templado, J Blanco, et al.
Human Reproduction (Oxford, England)|March 1, 1991
Chromosome abnormalities in human spermatozoa after albumin or TEST-Yolk capacitationJ Benet, J Navarro, A Genescà, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
A possible negative correlation between the frequency of chromosome lesions induced by folate-deficiency and age in individuals with the fra-Xq27.3 syndromeC Fuster, R Miró, C Templado, et al.
Human Genetics|June 1, 1986
G-banding of human sperm chromosomesJ Benet, A Genescà, J Navarro, et al.
International Journal of Andrology|February 1, 1982
Meiotic and synaptonemal complex studies in a 14/21 translocation carrierF Vidal, C Templado, J Navarro, et al.
Human Genetics|March 1, 1988
Concurrence of the triple-X syndrome and expression of the fragile site Xq27.3C Fuster, C Templado, R Miró, et al.
Human Reproduction (Oxford, England)|November 5, 1999
Paternal sex chromosome aneuploidy as a possible origin of Turner syndrome in monozygotic twins: case reportO Martínez-Pasarell, C Templado, E Vicens-Calvet, et al.
Pageof 6

Showing results (11-20 of 57) with videos related to

Sort By:
Pageof 6
Human Reproduction (Oxford, England)|October 1, 1987
Synaptonemal complex studies in the maleF Vidal, J Navarro, C Templado, et al.
Molecular Reproduction and Development|June 1, 1990
Effect of culture conditions and media on the frequency of chromosomal abnormalities in human sperm chromosome complementsR H Martin, C Templado, E Ko, et al.
Human Genetics|January 1, 1980
Meiotic studies in human semen. Report of 180 casesC Templado, S Marina, M D Coll, et al.
Human Genetics|April 3, 2001
Numerical chromosome abnormalities in the spermatozoa of the fathers of children with trisomy 21 of paternal origin: generalised tendency to meiotic non-disjunctionS R Soares, C Templado, J Blanco, et al.
Human Reproduction (Oxford, England)|March 1, 1991
Chromosome abnormalities in human spermatozoa after albumin or TEST-Yolk capacitationJ Benet, J Navarro, A Genescà, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
A possible negative correlation between the frequency of chromosome lesions induced by folate-deficiency and age in individuals with the fra-Xq27.3 syndromeC Fuster, R Miró, C Templado, et al.
Human Genetics|June 1, 1986
G-banding of human sperm chromosomesJ Benet, A Genescà, J Navarro, et al.
International Journal of Andrology|February 1, 1982
Meiotic and synaptonemal complex studies in a 14/21 translocation carrierF Vidal, C Templado, J Navarro, et al.
Human Genetics|March 1, 1988
Concurrence of the triple-X syndrome and expression of the fragile site Xq27.3C Fuster, C Templado, R Miró, et al.
Human Reproduction (Oxford, England)|November 5, 1999
Paternal sex chromosome aneuploidy as a possible origin of Turner syndrome in monozygotic twins: case reportO Martínez-Pasarell, C Templado, E Vicens-Calvet, et al.
Pageof 6