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C Bacino

Showing results (1-10 of 7) with videos related to

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American Journal of Medical Genetics|April 12, 2001
Atypical presentation of amniotic band sequenceO A Bodamer, E J Popek, C Bacino
Pharmacogenetics|June 1, 1995
Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafnessC Bacino, T R Prezant, X Bu, et al.
Annals of Human Genetics|October 1, 1988
A cytogenetic study of 47,XXY males of known origin and their parentsP A Jacobs, C Bacino, T Hassold, et al.
American Journal of Medical Genetics|May 8, 1999
Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two patients with Seckel syndromeF Abou-Zahr, B Bejjani, F A Kruyt, et al.
The Journal of Pediatrics|October 1, 1993
Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndromeS M Bernes, C Bacino, T R Prezant, et al.
JAMA|April 25, 1986
Human T-cell lymphotropic virus type III infection in a cohort of homosexual men in New York CityC E Stevens, P E Taylor, E A Zang, et al.
Orphanet Journal of Rare Diseases|June 14, 2015
De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformationsF J Probst, R A James, L C Burrage, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics|April 12, 2001
Atypical presentation of amniotic band sequenceO A Bodamer, E J Popek, C Bacino
Pharmacogenetics|June 1, 1995
Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafnessC Bacino, T R Prezant, X Bu, et al.
Annals of Human Genetics|October 1, 1988
A cytogenetic study of 47,XXY males of known origin and their parentsP A Jacobs, C Bacino, T Hassold, et al.
American Journal of Medical Genetics|May 8, 1999
Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two patients with Seckel syndromeF Abou-Zahr, B Bejjani, F A Kruyt, et al.
The Journal of Pediatrics|October 1, 1993
Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndromeS M Bernes, C Bacino, T R Prezant, et al.
JAMA|April 25, 1986
Human T-cell lymphotropic virus type III infection in a cohort of homosexual men in New York CityC E Stevens, P E Taylor, E A Zang, et al.
Orphanet Journal of Rare Diseases|June 14, 2015
De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformationsF J Probst, R A James, L C Burrage, et al.
Pageof 1