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R A Conte

Showing results (41-50 of 58) with videos related to

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Journal of Medical Genetics|November 14, 1997
Characterisation of a satellited non-fluorescent Y chromosome (Y[nfqs]) by FISHR S Verma, S K Gogineni, S M Kleyman, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1996
Mapping the homolog of the human Rb1 gene to chromosome 14 of higher primatesR S Verma, K H Ramesh, R V Samonte, et al.
Molecular & General Genetics : MGG|January 27, 1997
Unique genomic sequences in human chromosome 16p are conserved in the great apesS T Tarzami, A M Kringstein, R A Conte, et al.
Human Genetics|November 1, 1996
Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9R V Samonte, R A Conte, K H Ramesh, et al.
Clinical Genetics|November 1, 1992
Deciphering the fluorescent variability of human genomic heterochromatin by DA/DAPI techniqueR S Verma, R A Conte, S Luke, et al.
American Journal of Medical Genetics|July 1, 1994
Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosomeS Luke, R S Verma, R Giridharan, et al.
Annales De Genetique|January 1, 1996
Characterization of a de novo t(Y;9) (q11.2;q22) by FISH techniqueR A Conte, S M Kleyman, V Klein, et al.
Annales De Genetique|January 1, 1996
Centromeric alphoid sequences are breakage prone resulting in pericentromeric inversion heteromorphism of qh region of chromosome 1R S Verma, K H Ramesh, T Mathews, et al.
Annales De Genetique|January 1, 1997
Tandem duplication of chromosome 14 (q12q13)R S Verma, S M Kleyman, R A Conte, et al.
American Journal of Medical Genetics|February 11, 1997
Paracentric inversion involving the long arm of chromosome 9 resulting in deletion of abl geneS M Kleyman, A J Parekh, A R Rodriguez, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|November 14, 1997
Characterisation of a satellited non-fluorescent Y chromosome (Y[nfqs]) by FISHR S Verma, S K Gogineni, S M Kleyman, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1996
Mapping the homolog of the human Rb1 gene to chromosome 14 of higher primatesR S Verma, K H Ramesh, R V Samonte, et al.
Molecular & General Genetics : MGG|January 27, 1997
Unique genomic sequences in human chromosome 16p are conserved in the great apesS T Tarzami, A M Kringstein, R A Conte, et al.
Human Genetics|November 1, 1996
Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9R V Samonte, R A Conte, K H Ramesh, et al.
Clinical Genetics|November 1, 1992
Deciphering the fluorescent variability of human genomic heterochromatin by DA/DAPI techniqueR S Verma, R A Conte, S Luke, et al.
American Journal of Medical Genetics|July 1, 1994
Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosomeS Luke, R S Verma, R Giridharan, et al.
Annales De Genetique|January 1, 1996
Characterization of a de novo t(Y;9) (q11.2;q22) by FISH techniqueR A Conte, S M Kleyman, V Klein, et al.
Annales De Genetique|January 1, 1996
Centromeric alphoid sequences are breakage prone resulting in pericentromeric inversion heteromorphism of qh region of chromosome 1R S Verma, K H Ramesh, T Mathews, et al.
Annales De Genetique|January 1, 1997
Tandem duplication of chromosome 14 (q12q13)R S Verma, S M Kleyman, R A Conte, et al.
American Journal of Medical Genetics|February 11, 1997
Paracentric inversion involving the long arm of chromosome 9 resulting in deletion of abl geneS M Kleyman, A J Parekh, A R Rodriguez, et al.
Pageof 6