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Archives of Disease in Childhood|November 1, 1986
Dietary copper intake in artificially fed infantsS Salim, J Farquharson, G C Arneil, et al.
American Journal of Human Genetics|February 1, 1997
Sequence variation at the phenylalanine hydroxylase gene in the British IslesL A Tyfield, A Stephenson, F Cockburn, et al.
American Journal of Human Genetics|May 1, 1989
Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and SwitzerlandS E Sullivan, S D Moore, J M Connor, et al.
Investigative Genetics|September 25, 2012
High throughput DNA sequencing to detect differences in the subgingival plaque microbiome in elderly subjects with and without dementiaAndrew F Cockburn, Jonathan M Dehlin, Tiffany Ngan, et al.
Health Technology Assessment (Winchester, England)|January 1, 1997
Newborn screening for inborn errors of metabolism: a systematic reviewC A Seymour, M J Thomason, R A Chalmers, et al.
Pediatric Research|September 1, 1990
Biotin labeling of red cells in the measurement of red cell volume in preterm infantsI R Hudson, I A Cavill, A Cooke, et al.
Respiratory Medicine Case Reports|December 16, 2025
Cytotoxicity and virulence attributes of Pseudomonas aeruginosa isolates from case reports of patients with necrotizing pneumoniaT C Bolig, S H Nozick, C M R Axline, et al.
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