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T Lukusa

Showing results (21-30 of 33) with videos related to

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Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Role of gonadal dysgenesis in gonadoblastoma induction in 46, XY individuals. The Leuven experience in 46, XY pure gonadal dysgenesis and testicular feminization syndromesT Lukusa, J P Fryns, A Kleczkowska, et al.
Human Genetics|October 1, 1988
SCE variability in lymphocytes and fibroblasts. A controlled studyT Lukusa, P Vercauteren, H Van den Berghe, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Terminal 6q25.3 deletion and abnormal behaviourT Lukusa, D Willekens, N Lukusa, et al.
Genetic Counseling (Geneva, Switzerland)|August 6, 2005
Terminal 2q37 deletion and autistic behaviourT Lukusa, E Smeets, A Vogels, et al.
Genetic Counseling (Geneva, Switzerland)|July 23, 2003
Partial monosomy 11q and trisomy 12q: variable expression in two siblingsT Lukusa, M Holvoet, J R Vermeesch, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2004
Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorderT Lukusa, J R Vermeesch, M Holvoet, et al.
Cancer Genetics and Cytogenetics|October 1, 1990
No significant increase in spontaneous and ethyl methane sulfonate-induced sister chromatid exchanges at the Xq27.3 fragile siteT Lukusa, E Meulepas, J P Fryns, et al.
Human Genetics|September 1, 1991
"Spontaneous" FRA16B is a hot spot for sister chromatid exchangesT Lukusa, E Meulepas, J P Fryns, et al.
Annales De Genetique|January 9, 1999
Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1qT Lukusa, G Van Buggenhout, K Devriendt, et al.
Clinical Dysmorphology|April 5, 2019
Microdeletion of the entire IRF6 gene in a Subsaharian African's family with Van der Woude syndromeSébastien Mbuyi-Musanzayi, Eric I Kasamba, Nicole Revencu, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Role of gonadal dysgenesis in gonadoblastoma induction in 46, XY individuals. The Leuven experience in 46, XY pure gonadal dysgenesis and testicular feminization syndromesT Lukusa, J P Fryns, A Kleczkowska, et al.
Human Genetics|October 1, 1988
SCE variability in lymphocytes and fibroblasts. A controlled studyT Lukusa, P Vercauteren, H Van den Berghe, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Terminal 6q25.3 deletion and abnormal behaviourT Lukusa, D Willekens, N Lukusa, et al.
Genetic Counseling (Geneva, Switzerland)|August 6, 2005
Terminal 2q37 deletion and autistic behaviourT Lukusa, E Smeets, A Vogels, et al.
Genetic Counseling (Geneva, Switzerland)|July 23, 2003
Partial monosomy 11q and trisomy 12q: variable expression in two siblingsT Lukusa, M Holvoet, J R Vermeesch, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2004
Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorderT Lukusa, J R Vermeesch, M Holvoet, et al.
Cancer Genetics and Cytogenetics|October 1, 1990
No significant increase in spontaneous and ethyl methane sulfonate-induced sister chromatid exchanges at the Xq27.3 fragile siteT Lukusa, E Meulepas, J P Fryns, et al.
Human Genetics|September 1, 1991
"Spontaneous" FRA16B is a hot spot for sister chromatid exchangesT Lukusa, E Meulepas, J P Fryns, et al.
Annales De Genetique|January 9, 1999
Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1qT Lukusa, G Van Buggenhout, K Devriendt, et al.
Clinical Dysmorphology|April 5, 2019
Microdeletion of the entire IRF6 gene in a Subsaharian African's family with Van der Woude syndromeSébastien Mbuyi-Musanzayi, Eric I Kasamba, Nicole Revencu, et al.
Pageof 4