Literature DB >> 4866089

Genetic disease.

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Year:  1968        PMID: 4866089      PMCID: PMC1923868     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN: 0008-4409            Impact factor:   8.262


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  8 in total

1.  AN ALDOSTERONE BIOSYNTHETIC DEFECT IN A SALT-LOSING DISORDER.

Authors:  S ULICK; E GAUTIER; K K VETTER; J R MARKELLO; S YAFFE; C U LOWE
Journal:  J Clin Endocrinol Metab       Date:  1964-07       Impact factor: 5.958

2.  A gene locus concerned with hemolytic complement in Mus musculus.

Authors:  L A HERZENBERG; D K TACHIBANA; L A HERZENBERG; L T ROSENBERG
Journal:  Genetics       Date:  1963-05       Impact factor: 4.562

3.  Two cases of acatalasia in Switzerland.

Authors:  H AEBI; J P HEINIGER; R BUETLER; A HAESSIG
Journal:  Experientia       Date:  1961-10-15

4.  Specificity and inheritance of antibody response: a possible steering mechanism.

Authors:  B CINADER
Journal:  Nature       Date:  1960-11-19       Impact factor: 49.962

5.  [The allotype of certain blood protein antigens].

Authors:  J OUDIN
Journal:  C R Hebd Seances Acad Sci       Date:  1956-05-23

6.  Progressive oral gangrene probably due to lack of catalase in the blood (acatalasaemia); report of nine cases.

Authors:  S TAKAHARA
Journal:  Lancet       Date:  1952-12-06       Impact factor: 79.321

7.  Allotypy and eniotypy.

Authors:  B Cinader; S Dubiski; A C Wardlaw
Journal:  Nature       Date:  1966-06-18       Impact factor: 49.962

8.  Growth-hormone deficiency in man: an isolated, recessively inherited defect.

Authors:  D L Rimoin; T J Merimee; V A Mc Kusick
Journal:  Science       Date:  1966-06-17       Impact factor: 47.728

  8 in total

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