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M Rocchi

Showing results (211-220 of 309) with videos related to

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European Journal of Histochemistry : EJH|June 23, 2004
Localization of beta-defensin genes in non human primatesM Ventura, M Boniotto, M Pazienza, et al.
Human Genetics|October 30, 1999
X/Y translocation in a family with Leri-Weill dyschondrosteosisG Calabrese, R Fischetto, L Stuppia, et al.
Genomics|September 19, 2001
X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genesS Mumm, L Herrera, P W Waeltz, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1984
Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this siteP Szabo, M Purrello, M Rocchi, et al.
Journal of Neurology|May 1, 1995
Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patientsP Mandich, R James, S Nassani, et al.
American Journal of Human Genetics|March 1, 1985
Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybridsL Roncuzzi, S Fadda, M Mochi, et al.
Human Genetics|August 1, 1988
Relationship between the number and function of human ribosomal genesA de Capoa, M P Felli, A Baldini, et al.
Clinical Genetics|January 1, 1997
Two mosaic-YY males carrying asymmetric Y chromosomesL Zelante, B Dallapiccola, S Calvano, et al.
American Journal of Human Genetics|January 1, 1992
Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivationE Maestrini, S Rivella, C Tribioli, et al.
Oncogene|July 16, 2008
A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphomaL Impera, F Albano, C Lo Cunsolo, et al.
Pageof 31

Showing results (211-220 of 309) with videos related to

Sort By:
Pageof 31
European Journal of Histochemistry : EJH|June 23, 2004
Localization of beta-defensin genes in non human primatesM Ventura, M Boniotto, M Pazienza, et al.
Human Genetics|October 30, 1999
X/Y translocation in a family with Leri-Weill dyschondrosteosisG Calabrese, R Fischetto, L Stuppia, et al.
Genomics|September 19, 2001
X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genesS Mumm, L Herrera, P W Waeltz, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1984
Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this siteP Szabo, M Purrello, M Rocchi, et al.
Journal of Neurology|May 1, 1995
Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patientsP Mandich, R James, S Nassani, et al.
American Journal of Human Genetics|March 1, 1985
Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybridsL Roncuzzi, S Fadda, M Mochi, et al.
Human Genetics|August 1, 1988
Relationship between the number and function of human ribosomal genesA de Capoa, M P Felli, A Baldini, et al.
Clinical Genetics|January 1, 1997
Two mosaic-YY males carrying asymmetric Y chromosomesL Zelante, B Dallapiccola, S Calvano, et al.
American Journal of Human Genetics|January 1, 1992
Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivationE Maestrini, S Rivella, C Tribioli, et al.
Oncogene|July 16, 2008
A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphomaL Impera, F Albano, C Lo Cunsolo, et al.
Pageof 31