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I Voiculescu

Showing results (1-10 of 21) with videos related to

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Human Genetics|January 1, 1984
On the development of a standard two-dimensional polypeptide map of the human X chromosomeU Müller, I Voiculescu
Human Genetics|February 1, 1991
Homozygous condition for a BrdU-requiring fragile site on chromosome 12I Voiculescu, E Back, W Schempp
Chromosoma|January 1, 1972
[Karyotype and heterochromatin pattern in the Romanian hamster (Mesocricetus newtoni)]I Voiculescu, W Vogel, U Wolf
Revista De Pediatrie, Obstetrica Si Ginecologie. Pediatria|April 1, 1977
[Hereditary nigremia in children]M Burdea, A Tudoranu, I Voiculescu
Human Genetics|October 1, 1988
Deletion 11q23.3 without familial predispositionC Hausmann, E Back, G Wolff, et al.
Revista De Chirurgie, Oncologie, Radiologie, O. R. L., Oftalmologie, Stomatologie. Seria: Oftalmologie|October 1, 1988
[Exophthalmos due to ethmoidal and orbital mucocele]M Ivaşcu, G Vlase, I Voiculescu, et al.
Medicina Interna|August 1, 1971
[Meningitis with Escherichia coli (O119B14)]I Voiculescu, L Păun, L Sandu, et al.
Human Genetics|February 1, 1988
A BrdU-requiring fragile site on chromosome 12I Voiculescu, C Hausmann, G Wolff, et al.
Human Genetics|September 1, 1989
Familial ring (20) chromosomal mosaicismE Back, I Voiculescu, M Brünger, et al.
Acta Anthropogenetica|January 1, 1983
Exclusion of the C3 gene from the 19q133 to 19qter region by Southern analysis of human-rodent somatic cell hybrids, employing a cloned genomic C3 gene fragmentP Wieacker, G Fey, I Voiculescu, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Human Genetics|January 1, 1984
On the development of a standard two-dimensional polypeptide map of the human X chromosomeU Müller, I Voiculescu
Human Genetics|February 1, 1991
Homozygous condition for a BrdU-requiring fragile site on chromosome 12I Voiculescu, E Back, W Schempp
Chromosoma|January 1, 1972
[Karyotype and heterochromatin pattern in the Romanian hamster (Mesocricetus newtoni)]I Voiculescu, W Vogel, U Wolf
Revista De Pediatrie, Obstetrica Si Ginecologie. Pediatria|April 1, 1977
[Hereditary nigremia in children]M Burdea, A Tudoranu, I Voiculescu
Human Genetics|October 1, 1988
Deletion 11q23.3 without familial predispositionC Hausmann, E Back, G Wolff, et al.
Revista De Chirurgie, Oncologie, Radiologie, O. R. L., Oftalmologie, Stomatologie. Seria: Oftalmologie|October 1, 1988
[Exophthalmos due to ethmoidal and orbital mucocele]M Ivaşcu, G Vlase, I Voiculescu, et al.
Medicina Interna|August 1, 1971
[Meningitis with Escherichia coli (O119B14)]I Voiculescu, L Păun, L Sandu, et al.
Human Genetics|February 1, 1988
A BrdU-requiring fragile site on chromosome 12I Voiculescu, C Hausmann, G Wolff, et al.
Human Genetics|September 1, 1989
Familial ring (20) chromosomal mosaicismE Back, I Voiculescu, M Brünger, et al.
Acta Anthropogenetica|January 1, 1983
Exclusion of the C3 gene from the 19q133 to 19qter region by Southern analysis of human-rodent somatic cell hybrids, employing a cloned genomic C3 gene fragmentP Wieacker, G Fey, I Voiculescu, et al.
Pageof 3