Literature DB >> 4697852

Phenotypes of galactosaemia in infants screened at birth.

S Kelly, L Desjardins, P Armerding, J Burns.   

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Year:  1973        PMID： 4697852      PMCID： PMC1012972          DOI： 10.1136/jmg.10.1.27

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


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  6 in total

1.  A simple spot screening test for galactosemia.

Authors:  E Beutler; M C Baluda
Journal:  J Lab Clin Med       Date:  1966-07

2.  New rapid method for the estimation of red cell galactose-1-phosphate uridyl transferase activity.

Authors:  E Beutler; M Mitchell
Journal:  J Lab Clin Med       Date:  1968-09

3.  Screening for galactosemia in New York State.

Authors:  S Kelly; S Katz; J Burns; J Boylan
Journal:  Public Health Rep       Date:  1970-07       Impact factor: 2.792

4.  Improved method for measuring galactose-I-phosphate uridyl transferase activity of erythrocytes.

Authors:  E Beutler; M C Baluda
Journal:  Clin Chim Acta       Date:  1966-03       Impact factor: 3.786

5.  Electrophoretic variation of galactose-1-phosphate uridyltransferase.

Authors:  C K Mathai; E Beutler
Journal:  Science       Date:  1966-12-02       Impact factor: 47.728

6.  The genetics of galactose-1-phosphate uridyl transferase deficiency.

Authors:  E Beutler; M C Baluda; P Sturgeon; R W Day
Journal:  J Lab Clin Med       Date:  1966-10
  6 in total
  1 in total

1.  Problems affecting the community. Population screening.

Authors:  B E Clayton
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974
  1 in total

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