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American Journal of Medical Genetics
|
May 15, 1993
Poland anomaly with a limb body wall disruption defect
F J Stewart, N C Nevin, V E Boston
Clinical Genetics
|
September 1, 1993
Bilateral vocal cord paralysis in Williams syndrome
F 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 enzyme
F 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 fibrosis
P J Morrison, F J Stewart, A C Magee, et al.
Lancet (London, England)
|
August 5, 1998
Prevalence of tuberous sclerosis in UK
P 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 diagnosis
J 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 hyperphenylalaninaemia
J 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 trials
Kelly 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 symbionts
J G Sanders, R A Beinart, F J Stewart, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 36) with videos related to
Sort By:
Page
of 4
American Journal of Medical Genetics
|
May 15, 1993
Poland anomaly with a limb body wall disruption defect
F J Stewart, N C Nevin, V E Boston
Clinical Genetics
|
September 1, 1993
Bilateral vocal cord paralysis in Williams syndrome
F 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 enzyme
F 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 fibrosis
P J Morrison, F J Stewart, A C Magee, et al.
Lancet (London, England)
|
August 5, 1998
Prevalence of tuberous sclerosis in UK
P 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 diagnosis
J 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 hyperphenylalaninaemia
J 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 trials
Kelly 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 symbionts
J G Sanders, R A Beinart, F J Stewart, et al.
Page
of 4