Literature DB >> 5046627

Blood enzymes in the de Lange syndrome.

G F Smith, P Justice, D Y Hsia.   

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Year:  1972        PMID： 5046627      PMCID： PMC1469051          DOI： 10.1136/jmg.9.2.172

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  5 in total

1.  An in-vitro abnormality of glutathione metabolism in erythrocytes from normal newborns: mechanism and clinical significance.

Authors:  W H ZINKHAM
Journal:  Pediatrics       Date:  1959-01       Impact factor: 7.124

2.  Blood cell galactose-1-phosphate uridyl transferase activity in dysplastic patients, with and without chromosomal aberrations.

Authors:  A Dahlqvist; B Hall; B Källén
Journal:  Hum Hered       Date:  1969       Impact factor: 0.444

3.  Biochemical and genetic investigation of the de Lange syndrome.

Authors:  W L Daniel; J V Higgins
Journal:  Am J Dis Child       Date:  1971-05

Review 4.  Down's syndrome. A critical review of the biochemical and immunological data.

Authors:  D Y Hsia; G F Smith; R M Dowben; P Justice
Journal:  Am J Dis Child       Date:  1971-02

5.  An improved assay of erythrocyte and leukocyte galactose-1-phosphate uridyl transferase: stabilization of the enzyme by a thiol protective reagent.

Authors:  W J Mellman; T A Tedesco
Journal:  J Lab Clin Med       Date:  1965-12
  5 in total

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