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C C Talbot

Showing results (11-20 of 20) with videos related to

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American Journal of Human Genetics|June 1, 1993
Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14S E Antonarakis, J L Blouin, J Maher, et al.
Progress in Clinical and Biological Research|January 1, 1983
5-Azacytidine increases fetal hemoglobin production in a patient with sickle cell diseaseG J Dover, S H Charache, S H Boyer, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1979
Partial purification and characterization of DNA from the human X chromosomeB J Schmeckpeper, K D Smith, B P Dorman, et al.
BMC Genomics|April 5, 2022
Transcriptome analysis of blastoderms exposed to prolonged egg storage and short periods of incubation during egg storageK Brady, C C Talbot, J A Long, et al.
Human Genetics|August 11, 1991
Exclusion of linkage between familial Mediterranean fever and the human serum amyloid A (SAA) gene clusterG H Sack, C C Talbot, B G McCarthy, et al.
Human Molecular Genetics|July 1, 1995
The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cellsC C Talbot, D Avramopoulos, S Gerken, et al.
American Journal of Human Genetics|January 1, 1981
Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosisS R Panny, A F Scott, K D Smith, et al.
Neuroscience|March 25, 2014
MicroRNA-132 dysregulation in Toxoplasma gondii infection has implications for dopamine signaling pathwayJ Xiao, Y Li, E Prandovszky, et al.
Genomics|July 15, 1994
Two craniosynostotic syndrome loci, Crouzon and Jackson-Weiss, map to chromosome 10q23-q26X Li, A F Lewanda, F Eluma, et al.
American Journal of Human Genetics|November 11, 1992
DNA polymorphism analysis in families with recurrence of free trisomy 21C G Pangalos, C C Talbot, J G Lewis, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
American Journal of Human Genetics|June 1, 1993
Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14S E Antonarakis, J L Blouin, J Maher, et al.
Progress in Clinical and Biological Research|January 1, 1983
5-Azacytidine increases fetal hemoglobin production in a patient with sickle cell diseaseG J Dover, S H Charache, S H Boyer, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1979
Partial purification and characterization of DNA from the human X chromosomeB J Schmeckpeper, K D Smith, B P Dorman, et al.
BMC Genomics|April 5, 2022
Transcriptome analysis of blastoderms exposed to prolonged egg storage and short periods of incubation during egg storageK Brady, C C Talbot, J A Long, et al.
Human Genetics|August 11, 1991
Exclusion of linkage between familial Mediterranean fever and the human serum amyloid A (SAA) gene clusterG H Sack, C C Talbot, B G McCarthy, et al.
Human Molecular Genetics|July 1, 1995
The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cellsC C Talbot, D Avramopoulos, S Gerken, et al.
American Journal of Human Genetics|January 1, 1981
Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosisS R Panny, A F Scott, K D Smith, et al.
Neuroscience|March 25, 2014
MicroRNA-132 dysregulation in Toxoplasma gondii infection has implications for dopamine signaling pathwayJ Xiao, Y Li, E Prandovszky, et al.
Genomics|July 15, 1994
Two craniosynostotic syndrome loci, Crouzon and Jackson-Weiss, map to chromosome 10q23-q26X Li, A F Lewanda, F Eluma, et al.
American Journal of Human Genetics|November 11, 1992
DNA polymorphism analysis in families with recurrence of free trisomy 21C G Pangalos, C C Talbot, J G Lewis, et al.
Pageof 2