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H M Lewis

Showing results (51-60 of 55) with videos related to

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Archives of Disease in Childhood|May 1, 1979
A year's experience of the rotavirus syndrome and its association with respiratory illnessH M Lewis, J V Parry, H A Davies, et al.
Nucleic Acids Research|July 11, 1980
The complete amino acid sequence of human fibroblast interferon as deduced using synthetic oligodeoxyribonucleotide primers of reverse transcriptaseM Houghton, M A Easton, A G Stewart, et al.
Nucleic Acids Research|May 10, 1980
The amino-terminal sequence of human fibroblast interferon as deduced from reverse transcripts obtained using synthetic oligonucleotide primersM Houghton, A G Stewart, S M Doel, et al.
Nature Communications|January 14, 2015
Experimental evidence for the co-evolution of hominin tool-making teaching and languageT J H Morgan, N T Uomini, L E Rendell, et al.
Human Molecular Genetics|August 11, 1999
ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation classV L Ruiz-Perez, S A Carter, E Healy, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Archives of Disease in Childhood|May 1, 1979
A year's experience of the rotavirus syndrome and its association with respiratory illnessH M Lewis, J V Parry, H A Davies, et al.
Nucleic Acids Research|July 11, 1980
The complete amino acid sequence of human fibroblast interferon as deduced using synthetic oligodeoxyribonucleotide primers of reverse transcriptaseM Houghton, M A Easton, A G Stewart, et al.
Nucleic Acids Research|May 10, 1980
The amino-terminal sequence of human fibroblast interferon as deduced from reverse transcripts obtained using synthetic oligonucleotide primersM Houghton, A G Stewart, S M Doel, et al.
Nature Communications|January 14, 2015
Experimental evidence for the co-evolution of hominin tool-making teaching and languageT J H Morgan, N T Uomini, L E Rendell, et al.
Human Molecular Genetics|August 11, 1999
ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation classV L Ruiz-Perez, S A Carter, E Healy, et al.
Pageof 6