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H M Cann

Showing results (41-50 of 50) with videos related to

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Pediatrics|August 1, 1975
Inaccuracies in administering liquid medicationS J Yaffe, C W Bierman, H M Cann, et al.
Genomics|July 15, 1994
A YAC contig in 6p23 based on sequence tagged sitesM Nemani, D Cherif, H Chesne, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1983
Analysis of HLA class I genes with restriction endonuclease fragments: implications for polymorphism of the human major histocompatibility complexD Cohen, P Paul, M P Font, et al.
Pediatrics|February 1, 1973
Antihistamines in topical preparationsS J Yaffe, C W Bierman, H M Cann, et al.
Genomics|April 1, 1992
Genetic mapping of three human homologues of murine t-complex genes localizes TCP10 to 6q27, 15 cM distal to TCP1 and PLGH Blanché, L G Wright, G Vergnaud, et al.
American Journal of Human Genetics|July 1, 1991
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindredsH Y Zoghbi, C Jodice, L A Sandkuijl, et al.
Cytogenetics and Cell Genetics|January 1, 1985
Linkage relationships of the gene for the beta subunit of nerve growth factor (NGFB) with other chromosome 1 marker lociJ K Darby, J R Kidd, A J Pakstis, et al.
The New England Journal of Medicine|June 10, 1982
Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretionM L Batshaw, S Brusilow, L Waber, et al.
Genomics|April 16, 1998
CAG/CTG and CGG/GCC repeats in human brain reference cDNAs: outcome in searching for new dynamic mutationsV Albanese, S Holbert, C Saada, et al.
Human Molecular Genetics|July 1, 1996
Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disordersC Néri, V Albanèse, A S Lebre, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Pediatrics|August 1, 1975
Inaccuracies in administering liquid medicationS J Yaffe, C W Bierman, H M Cann, et al.
Genomics|July 15, 1994
A YAC contig in 6p23 based on sequence tagged sitesM Nemani, D Cherif, H Chesne, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1983
Analysis of HLA class I genes with restriction endonuclease fragments: implications for polymorphism of the human major histocompatibility complexD Cohen, P Paul, M P Font, et al.
Pediatrics|February 1, 1973
Antihistamines in topical preparationsS J Yaffe, C W Bierman, H M Cann, et al.
Genomics|April 1, 1992
Genetic mapping of three human homologues of murine t-complex genes localizes TCP10 to 6q27, 15 cM distal to TCP1 and PLGH Blanché, L G Wright, G Vergnaud, et al.
American Journal of Human Genetics|July 1, 1991
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindredsH Y Zoghbi, C Jodice, L A Sandkuijl, et al.
Cytogenetics and Cell Genetics|January 1, 1985
Linkage relationships of the gene for the beta subunit of nerve growth factor (NGFB) with other chromosome 1 marker lociJ K Darby, J R Kidd, A J Pakstis, et al.
The New England Journal of Medicine|June 10, 1982
Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretionM L Batshaw, S Brusilow, L Waber, et al.
Genomics|April 16, 1998
CAG/CTG and CGG/GCC repeats in human brain reference cDNAs: outcome in searching for new dynamic mutationsV Albanese, S Holbert, C Saada, et al.
Human Molecular Genetics|July 1, 1996
Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disordersC Néri, V Albanèse, A S Lebre, et al.
Pageof 5