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F J STEWART

Showing results (11-20 of 36) with videos related to

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American Journal of Medical Genetics|May 15, 1993
Poland anomaly with a limb body wall disruption defectF J Stewart, N C Nevin, V E Boston
Clinical Genetics|September 1, 1993
Bilateral vocal cord paralysis in Williams syndromeF J Stewart, M Dalzell, M McReid, et al.
Journal of Molecular Biology|May 2, 2000
Methyl-specific DNA binding by McrBC, a modification-dependent restriction enzymeF J Stewart, D Panne, T A Bickle, et al.
Clinical Genetics|August 1, 1994
Microcephaly with large anterior fontanelle, generalized convulsions, micropenis, and distinct anomalies of the hands and feet. Another example of Wiedemann syndrome?N C Nevin, F J Stewart, C W Corkey, et al.
Archives of Disease in Childhood|August 26, 1998
Confidential inquiry into families with two siblings with cystic fibrosisP J Morrison, F J Stewart, A C Magee, et al.
Lancet (London, England)|August 5, 1998
Prevalence of tuberous sclerosis in UKP J Morrison, C H Shepherd, F J Stewart, et al.
Human Mutation|January 1, 1994
Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosisJ Zschocke, C A Graham, F J Stewart, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Automated sequencing detects all mutations in Northern Irish patients with phenylketonuria and mild hyperphenylalaninaemiaJ Zschocke, C A Graham, F J Stewart, et al.
Trials|April 21, 2018
Stages of behavioural change after direct-to-consumer disease risk profiling: study protocol of two integrated controlled pragmatic trialsKelly F J Stewart, Anke Wesselius, Annemie M W J Schols, et al.
The ISME Journal|April 27, 2013
Metatranscriptomics reveal differences in in situ energy and nitrogen metabolism among hydrothermal vent snail symbiontsJ G Sanders, R A Beinart, F J Stewart, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|May 15, 1993
Poland anomaly with a limb body wall disruption defectF J Stewart, N C Nevin, V E Boston
Clinical Genetics|September 1, 1993
Bilateral vocal cord paralysis in Williams syndromeF J Stewart, M Dalzell, M McReid, et al.
Journal of Molecular Biology|May 2, 2000
Methyl-specific DNA binding by McrBC, a modification-dependent restriction enzymeF J Stewart, D Panne, T A Bickle, et al.
Clinical Genetics|August 1, 1994
Microcephaly with large anterior fontanelle, generalized convulsions, micropenis, and distinct anomalies of the hands and feet. Another example of Wiedemann syndrome?N C Nevin, F J Stewart, C W Corkey, et al.
Archives of Disease in Childhood|August 26, 1998
Confidential inquiry into families with two siblings with cystic fibrosisP J Morrison, F J Stewart, A C Magee, et al.
Lancet (London, England)|August 5, 1998
Prevalence of tuberous sclerosis in UKP J Morrison, C H Shepherd, F J Stewart, et al.
Human Mutation|January 1, 1994
Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosisJ Zschocke, C A Graham, F J Stewart, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Automated sequencing detects all mutations in Northern Irish patients with phenylketonuria and mild hyperphenylalaninaemiaJ Zschocke, C A Graham, F J Stewart, et al.
Trials|April 21, 2018
Stages of behavioural change after direct-to-consumer disease risk profiling: study protocol of two integrated controlled pragmatic trialsKelly F J Stewart, Anke Wesselius, Annemie M W J Schols, et al.
The ISME Journal|April 27, 2013
Metatranscriptomics reveal differences in in situ energy and nitrogen metabolism among hydrothermal vent snail symbiontsJ G Sanders, R A Beinart, F J Stewart, et al.
Pageof 4