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American Journal of Obstetrics and Gynecology|October 1, 1991
Does amniotic fluid index affect the accuracy of estimated fetal weight in preterm premature rupture of membranes?J S Toohey, D F Lewis, J A Harding, et al.
Journal of Medical Genetics|November 2, 2010
GeneScreen: a program for high-throughput mutation detection in DNA sequence electropherogramsIan M Carr, Nick Camm, Graham R Taylor, et al.
The Surgeon : Journal of the Royal Colleges of Surgeons of Edinburgh and Ireland|August 19, 2015
Postoperative exercise training is associated with reduced respiratory infection rates and early discharge: A case-control studyN R Bhatt, G Sheridan, M Connolly, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 18, 2009
Effect of progesterone on cervical shortening in women at risk for preterm birth: secondary analysis from a multinational, randomized, double-blind, placebo-controlled trialJ M O'Brien, E A Defranco, C D Adair, et al.
American Journal of Obstetrics and Gynecology|October 1, 1991
Rate of recurrence of preterm premature rupture of membranes in consecutive pregnanciesT Asrat, D F Lewis, T J Garite, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|January 10, 2002
Evaluation of 7-benzyloxy-4-trifluoromethylcoumarin, some other 7-hydroxy-4-trifluoromethylcoumarin derivatives and 7-benzyloxyquinoline as fluorescent substrates for rat hepatic cytochrome P450 enzymesA B Renwick, G Lavignette, P D Worboy, et al.
Human Mutation|November 5, 2011
Identification of autosomal recessive disease loci using out-bred nuclear familiesIan M Carr, Christine P Diggle, Nader Touqan, et al.
Electrophoresis|May 29, 2000
Construction and evaluation of a capillary array DNA sequencer based on a micromachined sheath-flow cuvetteH J Crabtree, S J Bay, D F Lewis, et al.
Toxicology|December 30, 1999
Molecular modelling of CYP1 family enzymes CYP1A1, CYP1A2, CYP1A6 and CYP1B1 based on sequence homology with CYP102D F Lewis, B G Lake, S G George, et al.
European Journal of Human Genetics : EJHG|February 26, 2022
Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher diseaseMarilena Elpidorou, James A Poulter, Katarzyna Szymanska, et al.
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