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O Zuffardi

Showing results (71-80 of 159) with videos related to

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Journal of Medical Genetics|October 1, 1989
Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorderH Rivera, O Zuffardi, P Maraschio, et al.
Human Genetics|October 1, 1990
Deletion of specific sequences or modification of centromeric chromatin are responsible for Y chromosome centromere inactivationP Maraschio, O Zuffardi, A Caiulo, et al.
American Journal of Human Genetics|June 30, 2001
Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndromeM C Bonaglia, R Giorda, R Borgatti, et al.
Journal of Medical Genetics|May 2, 2006
Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architectureR Ciccone, T Mattina, R Giorda, et al.
Clinical Genetics|June 14, 2000
A patient with maternal chromosome 14 UPD presenting with a mild phenotype and MODYM F Manzoni, T Pramparo, A Stroppolo, et al.
Journal of Medical Genetics|July 1, 1987
Translocation X;13 in a patient with retinoblastomaG Ponzio, E Savin, G Cattaneo, et al.
Chromosoma|September 28, 2000
A neocentromere in the DAZ region of the human Y chromosomeG Floridia, G Gimelli, O Zuffardi, et al.
Human Genetics|April 17, 1979
Familial XX true hermaphroditism and the H-Y antigenM Fraccaro, L Tiepolo, O Zuffardi, et al.
Journal of Medical Genetics|August 16, 2003
Distal trisomy 6p and 20q owing to the concurrent transposition of distal 6p and 20q to the 22q telomere: a genomic polymorphism?M C Bonaglia, R Giorda, A Cavallini, et al.
American Journal of Medical Genetics|February 1, 1985
Dup(3)(p2----pter) in two families, including one infant with cyclopiaG Gimelli, C Cuoco, M Lituania, et al.
Pageof 16

Showing results (71-80 of 159) with videos related to

Sort By:
Pageof 16
Journal of Medical Genetics|October 1, 1989
Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorderH Rivera, O Zuffardi, P Maraschio, et al.
Human Genetics|October 1, 1990
Deletion of specific sequences or modification of centromeric chromatin are responsible for Y chromosome centromere inactivationP Maraschio, O Zuffardi, A Caiulo, et al.
American Journal of Human Genetics|June 30, 2001
Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndromeM C Bonaglia, R Giorda, R Borgatti, et al.
Journal of Medical Genetics|May 2, 2006
Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architectureR Ciccone, T Mattina, R Giorda, et al.
Clinical Genetics|June 14, 2000
A patient with maternal chromosome 14 UPD presenting with a mild phenotype and MODYM F Manzoni, T Pramparo, A Stroppolo, et al.
Journal of Medical Genetics|July 1, 1987
Translocation X;13 in a patient with retinoblastomaG Ponzio, E Savin, G Cattaneo, et al.
Chromosoma|September 28, 2000
A neocentromere in the DAZ region of the human Y chromosomeG Floridia, G Gimelli, O Zuffardi, et al.
Human Genetics|April 17, 1979
Familial XX true hermaphroditism and the H-Y antigenM Fraccaro, L Tiepolo, O Zuffardi, et al.
Journal of Medical Genetics|August 16, 2003
Distal trisomy 6p and 20q owing to the concurrent transposition of distal 6p and 20q to the 22q telomere: a genomic polymorphism?M C Bonaglia, R Giorda, A Cavallini, et al.
American Journal of Medical Genetics|February 1, 1985
Dup(3)(p2----pter) in two families, including one infant with cyclopiaG Gimelli, C Cuoco, M Lituania, et al.
Pageof 16