Literature DB >> 2372606

An independent diagnosis.

T M Cox1.   

Abstract

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Substances：

Year:  1990        PMID： 2372606      PMCID： PMC1663185          DOI： 10.1136/bmj.300.6738.1512

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


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  2 in total

1.  Molecular architecture of rabbit skeletal muscle aldolase at 2.7-A resolution.

Authors:  J Sygusch; D Beaudry; M Allaire
Journal:  Proc Natl Acad Sci U S A       Date:  1987-11       Impact factor: 11.205

2.  Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.

Authors:  N C Cross; D R Tolan; T M Cox
Journal:  Cell       Date:  1988-06-17       Impact factor: 41.582
  2 in total
  2 in total

1.  Edit a staff round.

Authors:  R Winter
Journal:  BMJ       Date:  1991-11-16

2.  Adult hereditary fructose intolerance.

Authors:  Mohamed Ismail Yasawy; Ulrich Richard Folsch; Wolfgang Eckhard Schmidt; Michael Schwend
Journal:  World J Gastroenterol       Date:  2009-05-21       Impact factor: 5.742
  2 in total

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