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M J Pettenati

Showing results (21-30 of 87) with videos related to

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British Journal of Haematology|March 23, 1999
Identification of the inverted chromosome 16 using chromosome paintingP N Rao, W L Flejter, S Rahi, et al.
Genomics|June 1, 1996
Localization and physical mapping of genes encoding the A+U-rich element RNA-binding protein AUF1 to human chromosomes 4 and XB J Wagner, L Long, P N Rao, et al.
Cancer Genetics and Cytogenetics|November 1, 1988
Translocation (8;16)(p11;p13) in patients with acute monocytic leukemias. An evolving syndrome?B L Powell, J W McNay, S Brown, et al.
American Journal of Medical Genetics|April 1, 1989
Nonketotic hyperglycinemia in a patient with the 9p- syndromeB K Burton, M J Pettenati, S M Block, et al.
American Journal of Medical Genetics|May 1, 1991
Partial deletion of chromosome 6p: delineation of the syndromeC G Palmer, P Bader, M L Slovak, et al.
Human Genetics|August 1, 1994
Molecular cytogenetic analysis of a duplication Xp in a male: further delineation of a possible sex influencing region on the X chromosomeP N Rao, K Klinepeter, W Stewart, et al.
Clinical Genetics|September 17, 2003
Ring chromosome 17: phenotype variation by deletion sizeV Shashi, J R White, M J Pettenati, et al.
Cancer Genetics and Cytogenetics|July 15, 1994
Trisomy 5 as the sole abnormality in acute lymphoblastic leukemia. A second case and reviewP N Rao, D Buss, S Brown, et al.
Human Genetics|January 1, 1987
A heritable fragile 12q24.13 segregating in a family with the fragile X chromosomeA P Amarose, P R Huttenlocher, R M Sprudzs, et al.
Annals of Hematology|January 25, 2002
Primary malignant lymphoma of uterine corpus: case report and review of the literatureS I Renno, W S Moreland, M J Pettenati, et al.
Pageof 9

Showing results (21-30 of 87) with videos related to

Sort By:
Pageof 9
British Journal of Haematology|March 23, 1999
Identification of the inverted chromosome 16 using chromosome paintingP N Rao, W L Flejter, S Rahi, et al.
Genomics|June 1, 1996
Localization and physical mapping of genes encoding the A+U-rich element RNA-binding protein AUF1 to human chromosomes 4 and XB J Wagner, L Long, P N Rao, et al.
Cancer Genetics and Cytogenetics|November 1, 1988
Translocation (8;16)(p11;p13) in patients with acute monocytic leukemias. An evolving syndrome?B L Powell, J W McNay, S Brown, et al.
American Journal of Medical Genetics|April 1, 1989
Nonketotic hyperglycinemia in a patient with the 9p- syndromeB K Burton, M J Pettenati, S M Block, et al.
American Journal of Medical Genetics|May 1, 1991
Partial deletion of chromosome 6p: delineation of the syndromeC G Palmer, P Bader, M L Slovak, et al.
Human Genetics|August 1, 1994
Molecular cytogenetic analysis of a duplication Xp in a male: further delineation of a possible sex influencing region on the X chromosomeP N Rao, K Klinepeter, W Stewart, et al.
Clinical Genetics|September 17, 2003
Ring chromosome 17: phenotype variation by deletion sizeV Shashi, J R White, M J Pettenati, et al.
Cancer Genetics and Cytogenetics|July 15, 1994
Trisomy 5 as the sole abnormality in acute lymphoblastic leukemia. A second case and reviewP N Rao, D Buss, S Brown, et al.
Human Genetics|January 1, 1987
A heritable fragile 12q24.13 segregating in a family with the fragile X chromosomeA P Amarose, P R Huttenlocher, R M Sprudzs, et al.
Annals of Hematology|January 25, 2002
Primary malignant lymphoma of uterine corpus: case report and review of the literatureS I Renno, W S Moreland, M J Pettenati, et al.
Pageof 9