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R L Nussbaum

Showing results (61-70 of 115) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1988
Report of the committee on the genetic constitution of the X chromosomeJ L Mandel, H F Willard, R L Nussbaum, et al.
Advances in Experimental Medicine and Biology|January 1, 1984
Characterization and use of cloned sequences of the hypoxanthine-guanine phosphoribosyltransferase geneA C Chinault, J Brennand, D S Konecki, et al.
Developmental Biology|January 11, 2002
Disrupted sperm function and fertilin beta processing in mice deficient in the inositol polyphosphate 5-phosphatase Inpp5bE Hellsten, J P Evans, D J Bernard, et al.
Genomics|October 1, 1990
Partial deletions of a sequence family ("DXS278") and its physical linkage to steroid sulfatase as detected by pulsed-field gel electrophoresisR E Schnur, R G Knowlton, M A Musarella, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1987
Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardationR L Nussbaum, J G Lesko, R A Lewis, et al.
The Journal of Biological Chemistry|November 18, 2000
alpha-synuclein is phosphorylated by members of the Src family of protein-tyrosine kinasesC E Ellis, P L Schwartzberg, T L Grider, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Report of the committee on the genetic constitution of the X chromosomeK E Davies, J L Mandel, A P Monaco, et al.
American Journal of Human Genetics|February 1, 1989
New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridizationR E Schnur, S A Ledbetter, D H Ledbetter, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 1992
Isolation of a candidate gene for choroideremiaD E Merry, P A Jänne, J E Landers, et al.
The Journal of Pediatrics|June 1, 1990
Heterogeneity of clinical severity and molecular lesions in Aicardi syndromeJ A Neidich, R L Nussbaum, R J Packer, et al.
Pageof 12

Showing results (61-70 of 115) with videos related to

Sort By:
Pageof 12
Cytogenetics and Cell Genetics|January 1, 1988
Report of the committee on the genetic constitution of the X chromosomeJ L Mandel, H F Willard, R L Nussbaum, et al.
Advances in Experimental Medicine and Biology|January 1, 1984
Characterization and use of cloned sequences of the hypoxanthine-guanine phosphoribosyltransferase geneA C Chinault, J Brennand, D S Konecki, et al.
Developmental Biology|January 11, 2002
Disrupted sperm function and fertilin beta processing in mice deficient in the inositol polyphosphate 5-phosphatase Inpp5bE Hellsten, J P Evans, D J Bernard, et al.
Genomics|October 1, 1990
Partial deletions of a sequence family ("DXS278") and its physical linkage to steroid sulfatase as detected by pulsed-field gel electrophoresisR E Schnur, R G Knowlton, M A Musarella, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1987
Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardationR L Nussbaum, J G Lesko, R A Lewis, et al.
The Journal of Biological Chemistry|November 18, 2000
alpha-synuclein is phosphorylated by members of the Src family of protein-tyrosine kinasesC E Ellis, P L Schwartzberg, T L Grider, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Report of the committee on the genetic constitution of the X chromosomeK E Davies, J L Mandel, A P Monaco, et al.
American Journal of Human Genetics|February 1, 1989
New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridizationR E Schnur, S A Ledbetter, D H Ledbetter, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 1992
Isolation of a candidate gene for choroideremiaD E Merry, P A Jänne, J E Landers, et al.
The Journal of Pediatrics|June 1, 1990
Heterogeneity of clinical severity and molecular lesions in Aicardi syndromeJ A Neidich, R L Nussbaum, R J Packer, et al.
Pageof 12