D J Stalker|S Vigneswaren|P M Sharples|P W Lunt - JoVE Visualize

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British Medical Journal (Clinical Research Ed.)|November 22, 1986

Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophyA L Meredith, S M Huson, P W Lunt, et al.

Journal of Medical Genetics|September 8, 2001

Classification and genetic features of neonatal haemochromatosis: a study of 27 affected pedigrees and molecular analysis of genes implicated in iron metabolismA L Kelly, P W Lunt, F Rodrigues, et al.

Archives of Disease in Childhood|November 1, 1991

A practical method of serial bedside measurement of cerebral blood flow and metabolism during neurointensive careP M Sharples, A G Stuart, A Aynsley-Green, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999

The Opitz syndrome gene product, MID1, associates with microtubulesS Schweiger, J Foerster, T Lehmann, et al.

The Pediatric Infectious Disease Journal|January 6, 2001

Single dose pharmacokinetics of linezolid in infants and childrenG L Kearns, S M Abdel-Rahman, J L Blumer, et al.

Human Molecular Genetics|January 1, 1997

Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2M Oldridge, P W Lunt, E H Zackai, et al.

Archives of Disease in Childhood|June 27, 2009

Cerebral venous sinus thrombosis: a case series including thrombolysisA A Mallick, P M Sharples, S E Calvert, et al.

Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 17, 2001

Pharmacokinetics, metabolism, and excretion of linezolid following an oral dose of [(14)C]linezolid to healthy human subjectsJ G Slatter, D J Stalker, K L Feenstra, et al.

Acta Neuropathologica Communications|November 6, 2019

BRAF V600E mutation in Juvenile Xanthogranuloma family neoplasms of the central nervous system (CNS-JXG): a revised diagnostic algorithm to include pediatric Erdheim-Chester diseaseJ Picarsic, T Pysher, H Zhou, et al.

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Showing results (51-60 of 59) with videos related to

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You have reached the last page of results.This site can display upto 59 results.

British Medical Journal (Clinical Research Ed.)|November 22, 1986

Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophyA L Meredith, S M Huson, P W Lunt, et al.

Journal of Medical Genetics|September 8, 2001

Classification and genetic features of neonatal haemochromatosis: a study of 27 affected pedigrees and molecular analysis of genes implicated in iron metabolismA L Kelly, P W Lunt, F Rodrigues, et al.

Archives of Disease in Childhood|November 1, 1991

A practical method of serial bedside measurement of cerebral blood flow and metabolism during neurointensive careP M Sharples, A G Stuart, A Aynsley-Green, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999

The Opitz syndrome gene product, MID1, associates with microtubulesS Schweiger, J Foerster, T Lehmann, et al.

The Pediatric Infectious Disease Journal|January 6, 2001

Single dose pharmacokinetics of linezolid in infants and childrenG L Kearns, S M Abdel-Rahman, J L Blumer, et al.

Human Molecular Genetics|January 1, 1997

Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2M Oldridge, P W Lunt, E H Zackai, et al.

Archives of Disease in Childhood|June 27, 2009

Cerebral venous sinus thrombosis: a case series including thrombolysisA A Mallick, P M Sharples, S E Calvert, et al.

Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 17, 2001

Pharmacokinetics, metabolism, and excretion of linezolid following an oral dose of [(14)C]linezolid to healthy human subjectsJ G Slatter, D J Stalker, K L Feenstra, et al.

Acta Neuropathologica Communications|November 6, 2019

BRAF V600E mutation in Juvenile Xanthogranuloma family neoplasms of the central nervous system (CNS-JXG): a revised diagnostic algorithm to include pediatric Erdheim-Chester diseaseJ Picarsic, T Pysher, H Zhou, et al.

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