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Human genetics

Showing results (741-750 of 9,569) with videos related to

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Human Genetics|January 1, 1981
Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiencyJ P Fryns, M Azou, J Jaeken, et al.
Human Genetics|January 1, 1981
Mitotic and meiotic analysis of a reciprocal translocation t(Y;3) in an azoospermic maleJ Gonzales, S Lesourd, B Dutrillaux
Human Genetics|January 1, 1981
Duplication deficiency as the result of meiotic segregation of a maternal InV (10)E Yunis, O Torres de Caballero
Human Genetics|January 1, 1981
Structural differences in pericentric inversions. Application to a model of risk of recombinantsA Daniel
Human Genetics|January 1, 1981
Chromosomal investigations in epileptic children during long-term therapy with phenytoin or primidoneK J Esser, F Kotlarek, M Habedank, et al.
Human Genetics|December 1, 1989
G2 chromosomal radiosensitivity in families with ataxia-telangiectasiaY Shiloh, R Parshad, M Frydman, et al.
Human Genetics|December 1, 1989
Rate of chromosomal aberrations in prenatally detected hydrops fetalis and hygroma colliG Schwanitz, K Zerres, U Gembruch, et al.
Human Genetics|December 1, 1989
Prenatal enzymatic diagnosis of Krabbe disease (globoid-cell leukodystrophy) using chorionic villi. Pitfalls in the use of uncultured villiK Harzer, I Schuster
Human Genetics|December 1, 1989
Use of transgenic mice for the characterization of human alpha 1-acid glycoprotein (orosomucoid) variantsL Tomei, C B Eap, P Baumann, et al.
Human Genetics|December 1, 1989
Unusual chromosome 20 anomaly arising "de novo" to give dic(20)qsD Pimentel, P Alonso, J A Abrisqueta
Pageof 957

Showing results (741-750 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|January 1, 1981
Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiencyJ P Fryns, M Azou, J Jaeken, et al.
Human Genetics|January 1, 1981
Mitotic and meiotic analysis of a reciprocal translocation t(Y;3) in an azoospermic maleJ Gonzales, S Lesourd, B Dutrillaux
Human Genetics|January 1, 1981
Duplication deficiency as the result of meiotic segregation of a maternal InV (10)E Yunis, O Torres de Caballero
Human Genetics|January 1, 1981
Structural differences in pericentric inversions. Application to a model of risk of recombinantsA Daniel
Human Genetics|January 1, 1981
Chromosomal investigations in epileptic children during long-term therapy with phenytoin or primidoneK J Esser, F Kotlarek, M Habedank, et al.
Human Genetics|December 1, 1989
G2 chromosomal radiosensitivity in families with ataxia-telangiectasiaY Shiloh, R Parshad, M Frydman, et al.
Human Genetics|December 1, 1989
Rate of chromosomal aberrations in prenatally detected hydrops fetalis and hygroma colliG Schwanitz, K Zerres, U Gembruch, et al.
Human Genetics|December 1, 1989
Prenatal enzymatic diagnosis of Krabbe disease (globoid-cell leukodystrophy) using chorionic villi. Pitfalls in the use of uncultured villiK Harzer, I Schuster
Human Genetics|December 1, 1989
Use of transgenic mice for the characterization of human alpha 1-acid glycoprotein (orosomucoid) variantsL Tomei, C B Eap, P Baumann, et al.
Human Genetics|December 1, 1989
Unusual chromosome 20 anomaly arising "de novo" to give dic(20)qsD Pimentel, P Alonso, J A Abrisqueta
Pageof 957