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Clinical Biochemistry|October 1, 1994
Laboratory screening for genetic disorders and birth defectsF J BamforthAnnals of Clinical Biochemistry|September 1, 1987
Serum free thyroxine and free triiodothyronine concentrations in healthy fullterm, preterm and sick preterm neonatesR John, F J BamforthJournal of Medical Genetics|February 1, 1988
Alpha 1 antitrypsin deficiency due to Pi null: clinical presentation and evidence for molecular heterogeneityF J Bamforth, N A KalshekerAmerican Journal of Medical Genetics|May 15, 1994
Mirror-image dental fusion and discordance in monozygotic twinsG H Sperber, G A Machin, F J BamforthJournal of Clinical Pathology|April 1, 1985
Normal reference ranges for biochemical substances relating to renal, hepatic, and bone function in fetal and maternal plasma throughout pregnancyC F Moniz, K H Nicolaides, F J Bamforth, et al.Human Genetics|October 1, 1990
Molecular characterisation of two alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) Null(Newport) (Gly115----Ser) and (Pi) Z Wrexham (Ser-19----Leu)A Graham, N A Kalsheker, F J Bamforth, et al.American Journal of Physical Anthropology|December 3, 2005
Population affinities of Neolithic Siberians: a snapshot from prehistoric Lake BaikalK P Mooder, T G Schurr, F J Bamforth, et al.Clinical Biochemistry|December 1, 1990
Biochemical investigation of a child with molybdenum cofactor deficiencyF J Bamforth, J L Johnson, A G Davidson, et al.Human Genetics|December 1, 1989
Molecular characterisation of three alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) nullcardiff (Asp256----Val); PiMmalton (Phe51----deletion) and PiI (Arg39----Cys)A Graham, N A Kalsheker, C R Newton, et al.Pageof 1