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The Journal of Pediatrics|May 1, 1992
Outcome after developmental intervention in the neonatal intensive care unit for mothers of preterm infants with low socioeconomic statusS J Parker, L K Zahr, J G Cole, et al.
Epidemiology and Infection|April 1, 1987
Characterization of Streptococcus zooepidemicus (Lancefield group C) from human and selected animal infectionsM Barnham, G Cole, A Efstratiou, et al.
Archives of Family Medicine|November 26, 1997
Do physicians do as they say? The case of mammographyB G Saver, T R Taylor, J R Treadwell, et al.
Archives of Biochemistry and Biophysics|May 9, 1998
Active-site disruption in native Limulus hemocyanin and its subunits by disulfide-bond reductants: a chemical probe for the study of structure-function relationships in the hemocyaninsR Topham, S Tesh, G Cole, et al.
Clinical Chemistry|October 3, 1999
Selection, validation, standardization, and performance of a designated comparison method for HDL-cholesterol for use in the cholesterol reference method laboratory networkM M Kimberly, E T Leary, T G Cole, et al.
Journal of Medical Genetics|September 1, 1990
The clinical features of osteogenesis imperfecta resulting from a non-functional carboxy terminal pro alpha 1(I) propeptide of type I procollagen and a severe deficiency of normal type I collagen in tissuesW G Cole, P E Campbell, J G Rogers, et al.
The Journal of Bone and Joint Surgery. British Volume|January 1, 1989
Reliability of radiological measurements in the assessment of the child's hipN S Broughton, D I Brougham, W G Cole, et al.
Journal of Lipid Research|March 1, 1990
Genetic heterogeneity of plasma lipoproteins in the mouse: control of low density lipoprotein particle sizes by genetic factorsS Jiao, T G Cole, R T Kitchens, et al.
Journal of Pediatric Orthopedics|September 20, 2007
Treatment of open femur fractures in children: comparison between external fixator and intramedullary nailingLeonhard Erich Ramseier, Atul R Bhaskar, William G Cole, et al.
Journal of Medical Genetics|April 1, 1990
The clinical features of three babies with osteogenesis imperfecta resulting from the substitution of glycine by arginine in the pro alpha 1(I) chain of type I procollagenW G Cole, C W Chow, J G Rogers, et al.
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